ChemicalBook >?? ???? >?? ???>??? ?? ?? ???>? ?? ???>2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene
2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene
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2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene ??
- ???
- 103 °C
- ?? ?
- 438.3±40.0 °C(Predicted)
- ??
- 1.388
- ?? ??
- Keep in dark place,Sealed in dry,Room Temperature
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- DMSO(?? ???, ???), ??(?? ???,???)
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- InChI
- InChI=1S/C18H14BrFS/c1-12-2-5-15(19)10-14(12)11-17-8-9-18(21-17)13-3-6-16(20)7-4-13/h2-10H,11H2,1H3
- InChIKey
- VLRIERSBZHUCOW-UHFFFAOYSA-N
- SMILES
- C1(CC2=CC(Br)=CC=C2C)SC(C2=CC=C(F)C=C2)=CC=1
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- ?? ? ???? ?? (GHS)
| HS ?? | 2934999090 |
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2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene C??? ??, ??, ??
Synthesis
prepares 2-(4-fluorophenyl) thiophene III:Prepared by Grignard reagent: N 2under protection; magnesium chips (11.7g is added in the 500mL there-necked flask that thermometer, reflux condensing tube, constant pressure funnel be housed; 480mmol), THF (15.0mL), drips 2 p-Fluoro bromo benzenes; add the initiation reaction of 2 iodine post-heating; p-Fluoro bromo benzene (70.0g, 400mmol) is dissolved in THF (250mL), after under reflux, drip the THF solution of p-Fluoro bromo benzene; drip Bi Baowen backflow 2h, GC detection feedstock conversion complete.

Linked reaction: N 2under protection; in the 1000mL there-necked flask that thermometer, reflux condensing tube, constant pressure funnel be housed, add 2-bromothiophene (52.2g, 320mmol), under stirring, add two (methyl ethyl diketone) palladium (23.4mg; 0.0320mmol); THF (200mL), is heated to 50°C, the above-mentioned Grignard reagent prepared of rear dropping; drip to finish and be warming up to 60°C; insulation 1h, GC detect to raw material reaction complete, terminate reaction.System is cooled to 30°C, drips dilute hydrochloric acid (2M, 150mL) under ice-water bath, drips complete vigorous stirring 0.5h, removes ice-water bath and make system naturally rise to room temperature, stratification, water layer CH 2cl 2(100mL × 3) extract, merge organic phase saturated sodium-chloride 200mL to wash, rear drying, concentrating under reduced pressure obtain light tan solid, vacuum-drying to constant weight obtains 2-(4-fluorophenyl) thiophene III (57.4g, 312mmol), it is 98.5% that GC detects purity, and yield is 99.1%.
1H NMR(500MHz,CDCl 3)δ7.65~7.54(m,2H),7.33~7.22(m,2H),7.14~7.03(m,3H).Gc-Ms:178.1.
2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene ?? ?? ? ???
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2-(4-Fluorophenyl)-thiophene
(5-broMo-2-Methylphenyl)(5-(4-fluorophenyl)thiophen-2-yl)Methanone
4-bromo-2-(chloromethyl)-1-methylbenzene
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BORANE THF
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2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene ?? ??
???( 401)?? ??
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2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene ?? ??:
5-bromo-2-chloro-4’-ethoxydiphenylmethane
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4-(5-broMo-2-chlorobenzyl)phenol
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5-Iodo-2-methylbenzoic acid
Canagliflozin heMihydrate
LIPOPHILIC SEPHADEX
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BCP19353
Canagliflozin
5-Bromo-2-chlorobenzoic acid
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