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Dicyclohexylcarbodiimide → 3-(2,4,5-Trifluorophenyl)propyl-3-(5-trimethylsilyl-3-furyl)proprionate

HRID 345897
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HRID 345897 반응식
[CH3:1][Si:2]([CH3:14])([CH3:13])[C:3]1[O:7][CH:6]=[C:5]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])[CH:4]=1.[F:15][C:16]1[CH:21]=[C:20]([F:22])[C:19]([F:23])=[CH:18][C:17]=1[CH2:24][CH2:25][CH2:26]O.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.ClCCl>[F:15][C:16]1[CH:21]=[C:20]([F:22])[C:19]([F:23])=[CH:18][C:17]=1[CH2:24][CH2:25][CH2:26][O:11][C:10](=[O:12])[CH2:9][CH2:8][C:5]1[CH:4]=[C:3]([Si:2]([CH3:1])([CH3:13])[CH3:14])[O:7][CH:6]=1
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참가 물질

6

반응물 3

HCID 10868DicyclohexylcarbodiimideHCID 199916093-(2,4,5-Trifluorophenyl)propan-1-olHCID 199916153-(5-Trimethylsilyl-3-furyl)propionic acid

생성물 1

HCID 199915883-(2,4,5-Trifluorophenyl)propyl-3-(5-trimethylsilyl-3-furyl)proprionate

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매
HCID 6344
Dichloromethane
용매

실험 절차

A mixture of 3-(5-trimethylsilyl-3-furyl)propionic acid (61.3 mg, 0.29 mmol), 3-(2,4,5-trifluorophenyl)propan-1-ol (55 mg, 0.29 mmol), 1,3-dicyclohexylcarbodiimide (66 mg, 0.32 mmol) and 4-dimethylaminopyridine (10 mg) in dichloromethane (3 ml) was stirred at room temperature overnight (17 hours). Most of the solvent was evaporated and the residue was purified by preparative TLC (20×20 cm, 1000μ silica plate; developed with 10% ethyl ether/hexane). The title ester was obtained as a colorless oil.

후처리

  1. customMost of the solvent was evaporated
  2. customthe residue was purified by preparative TLC (20×20 cm, 1000μ silica plate; developed with 10% ethyl ether/hexane)

출처 및 근거

ORD 기록
ord-53e0dda9298646e2b5636d95420fe3e6
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05059611

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