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Borane → 2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol

HRID 2056721
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HRID 2056721 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C@H:10]([CH2:11][C:12](O)=[O:13])[O:9][CH2:8][CH2:7][C:6]=2[CH:15]=1.B.C(=O)([O-])[O-].[Na+].[Na+]>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C@H:10]([CH2:11][CH2:12][OH:13])[O:9][CH2:8][CH2:7][C:6]=2[CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6331BoraneHCID 10340Sodium CarbonateHCID 106357992-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acid

생성물 1

HCID 536878432-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 2-((1S)-6-bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acid (21.3 g, 78.6 mmol) in anhydrous THF (65 mL) under an atmosphere of nitrogen and cooled to 0° C., was added dropwise borane.THF complex in THF (1M) (94 mL, 94 mmol). After stirring for 1 h between 0 and 10° C., the reaction mixture was treated with aqueous sodium carbonate then extracted into toluene. The organic layer was washed with dilute aqueous hydrochloric acid, then concentrated in vacuo to give the title compound as a white solid.

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후처리

  1. extractionthen extracted into toluene
  2. washThe organic layer was washed with dilute aqueous hydrochloric acid
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c2052c3b95db415d840ea13208e9a876
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07335660B2

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