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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,4-Butanediol → 4-(2-Fluoro-5-bromobenzyloxy)butanol

HRID 1066815
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HRID 1066815 반응식
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[H-].[Na+].[F:9][C:10]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:11]=1[CH2:12]Br>CN(C)C=O>[F:9][C:10]1[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:11]=1[CH2:12][O:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6]
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참가 물질

5

반응물 3

HCID 80641,4-ButanediolHCID 24758Sodium hydrideHCID 135532954-Bromo-2-(bromomethyl)-1-fluorobenzene

생성물 1

HCID 211961624-(2-Fluoro-5-bromobenzyloxy)butanol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 1,4-dihydroxybutane (4.0 ml, 45.13 mmol) in N,N-dimethylformamide (62 ml) was treated with sodium hydride (1.98 g of a 60% solution, 49.63 mmol), and stirred for about 50 minutes at ambient temperature. The resulting mixture was cooled to 0° C. and treated with 2-fluoro-5-bromobenzyl bromide (3.0 g, 11.28 mmol). The reaction mixture was then stirred for four hours at ambient temperature. The reaction was quenched with water. The aqueous fraction was extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The desired title intermediate was further purified by high performance liquid chromatography.

후처리

  1. temperatureThe resulting mixture was cooled to 0° C.
  2. stirringThe reaction mixture was then stirred for four hours at ambient temperature
  3. customThe reaction was quenched with water
  4. extractionThe aqueous fraction was extracted with methylene chloride
  5. dry with materialdried over sodium sulfate
  6. customThe solvents were removed in vacuo
  7. customThe desired title intermediate was further purified by high performance liquid chromatography

출처 및 근거

ORD 기록
ord-96ffe5c3cac14f118bd24bd99d6196d6
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06245761B1

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