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Carbon Dioxide → HCID 13070643, 화합물

HRID 1576255
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반응식

HRID 1576255 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:14]=[CH:15][CH:16]=1)[CH:6]([OH:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C([Li])CCC.[C:22](=O)=[O:23]>CCOCC.CCCCCC>[CH3:1][O:2][C:3]1[CH:16]=[CH:15][CH:14]=[C:5]2[C:4]=1[C:22](=[O:23])[O:13][CH:6]2[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 280Carbon Dioxide2회HCID 573301(3-Methoxyphenyl)(phenyl)methanolHCID 178418339Butyllithium

생성물 1

HCID 13070643HCID 13070643, 화합물

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 8058Hexane용매

실험 절차

To 3-methoxybenzhydrol (42.8 g.) in dry ether (800 ml.) is added 2.3 M. n-butyl lithium in hexane (250 ml.), dropwise with stirring under nitrogen. The deep red solution is stirred and heated under reflux for 2 hours and then poured into a stirred slurry of a large excess of solid carbon dioxide in ether and stirred until no carbon dioxide remains. The resulting suspension is extracted with water, the extract is acidified with concentrated hydrochloric acid, the precipitate is filtered off, washed with water, dried, and recrystallised from isopropanol to give 7-methoxy-3-phenylphthalide, m.p. 135°-138°C.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 2 hours
  3. extractionThe resulting suspension is extracted with water
  4. filtrationthe precipitate is filtered off
  5. washwashed with water
  6. customdried
  7. customrecrystallised from isopropanol

출처 및 근거

ORD 기록
ord-dd73aa6131d246759bd8e5fd057c0a21
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03979513

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