Ethyl Acetate → (1-Naphthalen-1-yl-cyclopentyl)-methanol

HRID 2169375ノート

反応式

HRID 2169375 の反応式
[C:1]1([C:11]2([CH:16]=[O:17])[CH2:15][CH2:14][CH2:13][CH2:12]2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+].C(OCC)(=O)C>CO.CCCCCC>[C:1]1([C:11]2([CH2:16][OH:17])[CH2:15][CH2:14][CH2:13][CH2:12]2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

参加物

6

実験手順

A solution of 1-naphthalen-1-yl-cyclopentanecarbaldehyde (339) (10 g, 44.6 mmol) in methanol (150 mL) was cooled to 0° C. and NaBH4 (3.373 g, 89.2 mmol) was added in portions (8 portions). After the addition was completed the reaction mixture was allowed to stir at room temperature for 1 h (silica TLC, 10% ethyl acetate in hexane; Rf=0.3). The reaction mixture was quenched with aqueous NH4Cl solution and concentrated in vacuo as much as possible; diluted with water (100 mL) and extracted with ethyl acetate (2×100 mL). The organic part was washed with brine (50 mL), dried and concentrated in vacuo to get a crude mass which was purified by CombiFlash using gradient eluent mixture of ethyl acetate and hexane to get pure (1-naphthalen-1-yl-cyclopentyl)-methanol (340) (8.75 g, 87%) as a white solid.

後処理

  1. additionAfter the addition
  2. customThe reaction mixture was quenched with aqueous NH4Cl solution
  3. concentrationconcentrated in vacuo as much as possible
  4. additiondiluted with water (100 mL)
  5. extractionextracted with ethyl acetate (2×100 mL)
  6. washThe organic part was washed with brine (50 mL)
  7. customdried
  8. concentrationconcentrated in vacuo
  9. customto get a crude mass which
  10. customwas purified by CombiFlash
  11. additiongradient eluent mixture of ethyl acetate and hexane

出典と根拠

ORDレコード
ord-e97c1d41c3ab45fab97743e21e9c19ee
出典データセット
uspto-grants-2015_06
特許番号
US09045486B2

反応ノート

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