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tert-Butyl acrylate → 3-[2-(4-Hydroxy-phenyl)-morpholin-4-yl]-propionic acid tert-butyl ester

HRID 588248
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인쇄 미리보기

반응식

HRID 588248 반응식
[NH:1]1[CH2:6][CH2:5][O:4][CH:3]([C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)[CH2:2]1.[C:14]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])(=[O:17])[CH:15]=[CH2:16]>CC#N>[C:19]([O:18][C:14](=[O:17])[CH2:15][CH2:16][N:1]1[CH2:6][CH2:5][O:4][CH:3]([C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)[CH2:2]1)([CH3:22])([CH3:21])[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 15458tert-Butyl acrylateHCID 538045794-(Morpholin-2-yl)phenol

생성물 1

HCID 666540623-[2-(4-Hydroxy-phenyl)-morpholin-4-yl]-propionic acid tert-butyl ester수율 77.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 4-morpholin-2-yl-phenol (3.95 g; 22.0 mmol), and tert-butyl acrylate (9.60 mL; 66.1 mmol) in CH3CN (100 mL) was heated under reflux overnight. After cooling to RT, the mixture was concentrated and purified by column chromatography (SiO2, Et2O) to afford 3-[2-(4-hydroxy-phenyl)-morpholin-4-yl]-propionic acid tert-butyl ester (5.22 g).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux overnight
  3. concentrationthe mixture was concentrated
  4. custompurified by column chromatography (SiO2, Et2O)

출처 및 근거

ORD 기록
ord-fef93bf0d1104a338e33bbc51ec2206d
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227960B2

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