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Benzyl vinylcarbamate

Benzyl vinylcarbamate Struktur
84713-20-2
CAS-Nr.
84713-20-2
Englisch Name:
Benzyl vinylcarbamate
Synonyma:
benzyl vinylcarbamate;O-Benzyl-N-vinylcarbamate;N-Cbz-ethenamine;BENZYL-N-VINYLCARBAMATE;benzyl ethenylcarbamate;N-vinyl benzyl carbamate;N-Vinyl-O-benzyl urethane;benzyl N-ethenylcarbamate;Phenylmethyl ethenylcarbamate;N-ethyleneylaminomacetic acidbenzyl ester
CBNumber:
CB1679005
Summenformel:
C10H11NO2
Molgewicht:
177.2
MOL-Datei:
84713-20-2.mol

Benzyl vinylcarbamate Eigenschaften

Schmelzpunkt:
43-44°C
Siedepunkt:
272℃
Dichte
1.089
Flammpunkt:
118℃
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
L?slichkeit
Chloroform (Slightly), Ethyl Acetate (Slightly)
Aggregatzustand
Solid
pka
11.04±0.46(Predicted)
Farbe
White to Off-White
InChI
InChI=1S/C10H11NO2/c1-2-11-10(12)13-8-9-6-4-3-5-7-9/h2-7H,1,8H2,(H,11,12)
InChIKey
YGBQZFPEMRCQRY-UHFFFAOYSA-N
SMILES
C(OCC1=CC=CC=C1)(=O)NC=C
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
R-S?tze: 36/37/38
S-S?tze: 26-36/37/39
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Benzyl vinylcarbamate Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-S?tze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.

synthetische

A 1-L flask was equipped with a variable speed pump, a mechanical stirrer, a temperature controller, a 4" (10 cm) column packed with ceramic saddles, a distillation head, a spiral condenser (cooled with water at 10–15 ℃), and a receiver. The flask was charged with toluene (150–200 mL) and phenothiazine (0.5 g) and the solution was heated to 105–110 ℃. The receiver was charged with benzyl alcohol (86 g, 0.8 mol), phenothiazine (0.05 g), and triethylamine (0.1–0.3 g). This mixture was cooled in ice and stirred. A solution of acryloyl azide (1 mol), prepared as described above, was pumped into the distillation flask over a period of 4–5 h, maintaining the pot temperature at 105–110 ℃ with a heating mantle. The vapor temperature varied, depending on the rate of addition of the azide, but was in the range 80–100 ℃. The distillate was passed directly into the benzyl alcohol mixture. After the addition of acryloyl azide, the distillation continued, generating a further 10–20 mL of toluene. The receiver was then removed from the distillation set-up, and its contents were stirred at 0–5 ℃ for 1– 2 h. The product mixture was then allowed to gradually warm to room temperature and was stirred until HPLC analysis indicated complete reaction. The mixture was then concentrated in vacuo to a weight of 200–250 g. The residue was treated with heptane (300–350 mL) and cooled to 15 ℃ with stirring. A few seed crystals of benzyl N-vinyl carbamate 810 were added, and the mixture was stirred for 2–3 h. The product was collected by filtration, washed with heptane, and dried in vacuo. Yield 115–128 g (65–72%); mp 41–44 ℃.

Application

Benzyl-N-vinyl carbamate (Z-vinylamine; Benzyl vinylcarbamate) is a valuable synthetic intermediate. This compound undergoes alkylation readily on the carbon R to the nitrogen, a property that has been used in the synthesis of a-lactam antibiotics. Z-vinylamine can be readily polymerized into polyvinyl amine derivatives[1].

Synthesis Reference(s)

The Journal of Organic Chemistry, 54, p. 4649, 1989 DOI: 10.1021/jo00280a036

Benzyl vinylcarbamate Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Benzyl vinylcarbamate Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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  • N-Vinyl-O-benzyl urethane
  • BENZYL-N-VINYLCARBAMATE
  • Phenylmethyl ethenylcarbamate
  • benzyl N-ethenylcarbamate
  • Carbamic acid, N-ethenyl-, phenylmethyl ester
  • benzyl ethenylcarbamate
  • benzyl vinylcarbamate
  • N-Cbz-ethenamine
  • Benzyl vinylcarbamate,98% (stabilized with TBC)
  • N-vinyl benzyl carbamate
  • N-ethyleneylaminomacetic acidbenzyl ester
  • O-Benzyl-N-vinylcarbamate
  • 84713-20-2
  • organic building block
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