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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Bromo(phenyl)acetic acid → 2-Bromo-2-phenylethanol

HRID 34833
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인쇄 미리보기

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HRID 34833 반응식
[Br:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:3](O)=[O:4].B#B.O1CCCC1.O>O1CCCC1>[Br:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH2:3][OH:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 97919Bromo(phenyl)acetic acidHCID 6328200DiboronHCID 21881883Oxolane--water (1/1)

생성물 1

HCID 5783322-Bromo-2-phenylethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a stirred solution of 25 g of α-bromphenylacetic acid in 100 ml of dry tetrahydrofuran was added 151 ml of 1.0M diborane in tetrahydrofuran dropwise at 5° C. under argon over 30 minutes. This mixture was stirred overnight at room temperature, then cooled to 0° C. and 130 ml of tetrahydrofuran:water (1:1) was added dropwise. The mixture was then saturated with potassium carbonate and the tetrahydrofuran removed. The aqueous remainder was extracted three times with ether. The extracts were combined and dried. The residue was triturated with hexane and the solid collected giving the desired compound as white needles, mp 38°-39° C.

후처리

  1. temperaturecooled to 0° C.
  2. customsaturated with potassium carbonate and the tetrahydrofuran removed
  3. extractionThe aqueous remainder was extracted three times with ether
  4. customdried
  5. customThe residue was triturated with hexane
  6. customthe solid collected

출처 및 근거

ORD 기록
ord-b0f3831dca3c442fb30e53f98498613d
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04762942

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