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(-)-Dibenzoyl-L-tartaric acid monohydrate

(-)-Dibenzoyl-L-tartaric acid monohydrate ??? ???
?? ??:
62708-56-9
???:
(-)-Dibenzoyl-L-tartaric acid monohydrate
???(??):
L-DBTA;DIBENZOYL-L-TARTARIC ACID MONOHYDRATE;O,O'-Dibenzoyl-d-Tartaric acid Anhydrous;(+)-Dibenzoyl-L-tartaric acid monohydrate;(-)-O,O'-Dibenzoyl-L-tartaric acid monohydrate;(2S,3S)-2,3-bis(benzoyloxy)succinic acid hydrate;L-(-)-DBTA H2O;L-(-)-DBTA.2H2O;(-)-O,O'-DibenzoyL;(-)-Dibenzoyl-L-tart
CBNumber:
CB6310345
???:
C18H16O9
??? ??:
376.31
MOL ??:
62708-56-9.mol
MSDS ??:
SDS

(-)-Dibenzoyl-L-tartaric acid monohydrate ??

???
88-89 °C(lit.)
??
-115 º (c=5, ethanol)
???
-108.5 ° (C=1, EtOH)
?? ??
Store below +30°C.
??? ??
??
??
???
?? ??
[α]20/D 110±3°, c = 5% in ethanol
???
??
BRN
4065263
InChI
InChI=1/C18H14O8.H2O/c19-15(20)13(25-17(23)11-7-3-1-4-8-11)14(16(21)22)26-18(24)12-9-5-2-6-10-12;/h1-10,13-14H,(H,19,20)(H,21,22);1H2/t13-,14-;/s3
InChIKey
DXDIHODZARUBLA-DTPOWOMPSA-N
SMILES
[C@@H](C(=O)O)(OC(=O)C1C=CC=CC=1)[C@H](C(=O)O)OC(=O)C1C=CC=CC=1.O |&1:0,13,r|
CAS ??????
62708-56-9(CAS DataBase Reference)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi
?? ???? ?? 36
????? 26-36-37/39
WGK ?? 3
RTECS ?? WW8070000
F ?????? 3
TSCA Yes
HS ?? 29181990
???? ??? 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? P264, P280, P305+P351+P338,P337+P313P
??????:
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
1
2 0

(-)-Dibenzoyl-L-tartaric acid monohydrate C??? ??, ??, ??

??? ??

white to light yellow crystal powde

??

(-)-Dibenzoyl-L-tartaric acid is used as an intermediate in pharmaceutical and agro chemical industries. It is used as chiral auxiliary in organic synthesis and as a resolution agent in the synthesis of rameleton.

?? ??

(-)-O,O′-Dibenzoyl-L-tartaric acid monohydrate may be used as a chiral resolving agent for the resolution of racemic bioactive compounds such as (±)-3-(3-hydroxyphenyl)-N-(1-propyl)-piperidine and (±)-2-(5,6-dimethoxy-1,2,3,4-tetrahydro-1-naphthyl)-imidazoline to isolate the corresponding (-)-enantiomeric forms.

Purification Methods

Crystallise the acid from water (18g from 400 mL boiling H2O) and stir vigorously while cooling in order to obtain crystals; otherwise an oil will separate which solidifies on cooling. Dry it in a vacuum desiccator over KOH/H2SO4 (yield 16.4g) as monohydrate, m 88-89o. It crystallises from xylene as the anhydrous acid, m 173o (150-153o). It does not crystallise from *C6H6, toluene, *C6H6/pet ether (oil), or CHCl3/pet ether. [Butler & Cretcher J Am Chem Soc 55 2605 1933, Acs et al. Tetrahedron 41 2465 1985, R(+) Beilstein 9 IV 557, S(-) Beilstein 9 III 870.]

(-)-Dibenzoyl-L-tartaric acid monohydrate ?? ?? ? ???

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(-)-Dibenzoyl-L-tartaric acid monohydrate ?? ??

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(-)-Dibenzoyl-L-tartaric acid monohydrate ?? ??:

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