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Water → HCID 22795184, 화합물

HRID 1973685
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HRID 1973685 반응식
C[O:2][C:3]1[CH:4]=[C:5]([C@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]2[N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)[CH:6]=[CH:7][CH:8]=1.B(Br)(Br)Br.O>ClCCl>[OH:2][C:3]1[CH:4]=[C:5]([C@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]2[N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 53847304HCID 53847304, 화합물

생성물 1

HCID 22795184HCID 22795184, 화합물수율 84.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

(2) A solution of cis-2-(3-methoxyphenyl)-1-pyrrolidinocyclohexane (2.5g) in dichloromethane was added cautiously to an ice-cold solution of boron tribromide (3 ml) in dichloromethane (15 ml). The mixture was set aside at room temperature for 18 hours and was hydrolysed with water. The aqueous layer was collected, made alkaline with ammonia and extracted with ether. The ether extracts were washed, dried (Na2SO4) and evaporated. The residue was crystallised from aqueous ethanol to give cis-2-(3-hydroxyphenyl)-1-pyrrolidinocyclohexane (2.0g), m.p. 125° to 127° C, identical to (b)(1) above.

후처리

  1. customThe aqueous layer was collected
  2. extractionextracted with ether
  3. washThe ether extracts were washed
  4. dry with materialdried (Na2SO4)
  5. customevaporated
  6. customThe residue was crystallised from aqueous ethanol

출처 및 근거

ORD 기록
ord-c8ed6634821f47539eb22fa33da6407a
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03998843

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