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Dichloromethane → HCID 21112933, 화합물

HRID 1767204
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반응식

HRID 1767204 반응식
C([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]2[CH2:15][CH2:14][CH2:13][C:12]=2[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[O:22]C)[CH:6]=1)C.ClCCl>B(Br)(Br)Br>[OH:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[C:12]1[CH2:13][CH2:14][CH2:15][C:11]=1[C:7]1[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=1)[C:4]([OH:24])=[O:3]
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참가 물질

4

반응물 2

HCID 6344DichloromethaneHCID 695079153-[2-(2-Methoxy-phenyl)-cyclopent-1-enyl]-benzoic Acid Ethyl Ester

생성물 1

HCID 21112933HCID 21112933, 화합물

시약·촉매·용매 1

HCID 25134Boron tribromide용매

실험 절차

3-[2-(2-Methoxy-phenyl)-cyclopent-1-enyl]-benzoic acid ethyl ester (610 mg, 1.89 mmol) was dissolved in 1M boron tribromide in dichloromethane solution (18.9 ml, 18.9 mmol) and left at room temperature for 18 hours. The resulting solution was poured onto ice and extracted with dichloromethane. The organic extract was dried (MgSO4), evaporated to dryness and purified by chromatography using biotage with iso-hexane containing a gradient of ethyl acetate (20–40%) to yield the title compound as a light brown solid. (186 mg, 35%).

후처리

  1. additionThe resulting solution was poured onto ice
  2. extractionextracted with dichloromethane
  3. extractionThe organic extract
  4. dry with materialwas dried (MgSO4)
  5. customevaporated to dryness
  6. custompurified by chromatography

출처 및 근거

ORD 기록
ord-072be2acd1d542d4a01122db1c92107b
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07232821B2

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