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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
ノート
印刷プレビュー

反応式

HRID 2056750 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

(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).

後処理

  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

出典と根拠

ORDレコード
ord-979dfce3043c4d37a2d9a222ef4b9e10
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07335660B2

反応ノート

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