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2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid → 2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanol

HRID 2056750
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HRID 2056750 반응식
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]2[CH:6]([CH2:9][C:10](O)=[O:11])[O:7][CH2:8][C:4]=2[CH:3]=1>C1COCC1>[Cl:1][C:2]1[CH:14]=[CH:13][C:5]2[CH:6]([CH2:9][CH2:10][OH:11])[O:7][CH2:8][C:4]=2[CH:3]=1
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참가 물질

3

반응물 1

HCID 693078062-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid

생성물 1

HCID 693065152-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid (1.91 g, 9.0 mmol) was dissolved in dry THF (8 mL) under nitrogen and cooled to 0° C. Borane-dimethylsulfide complex (0.155 mL, 1.64 mmol) was added by syringe. After 1 h the cooling bath was removed and the solution was stirred at room temperature for 2 h. The solution was partitioned between saturated aqueous sodium hydrogen carbonate and diethyl ether. The aqueous layer was further extracted with ether, and the combined organic layers washed with brine, dried (MgSO4), filtered and concentrated in vacuo. This yielded the title compound as a white solid (>98% ee by chiral HPLC).

후처리

  1. additionBorane-dimethylsulfide complex (0.155 mL, 1.64 mmol) was added by syringe
  2. customAfter 1 h the cooling bath was removed
  3. customThe solution was partitioned between saturated aqueous sodium hydrogen carbonate and diethyl ether
  4. extractionThe aqueous layer was further extracted with ether
  5. washthe combined organic layers washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-979dfce3043c4d37a2d9a222ef4b9e10
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07335660B2

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