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Acetic Acid → HCID 11841701、化合物

HRID 904822
ノート
印刷プレビュー

反応式

HRID 904822 の反応式
[C:1]([NH:4][CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]1=[O:15])(=[O:3])[CH3:2].[BH4-].[Na+].C(O)(=O)C>C(O)C>[C:1]([NH:4][C@@H:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C@H:6]1[OH:15])(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 176Acetic AcidHCID 4311764Sodium borohydrideHCID 9859076HCID 9859076、化合物

生成物 1

HCID 11841701HCID 11841701、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of the 2-acetamido-3,4-dihydronaphthalen-1(2H)-one from Step A in absolute ethanol (150 ml) was added sodium borohydride (2.0 gms, 0.05 m) in portions. The reaction mixture was stirred at room temperature for 1/2 hour. Acetic acid was added dropwise to destroy the excess sodium borohydride. The reaction mixture was poured into water and extracted with ethyl acetate (3×150 ml). The ethyl acetate was washed with saturated aqueous sodium chloride (150 ml) and dried over anhydrous sodium sulfate. After filtration the solvent was removed under reduced pressure to yield 5.5 gms (54%, over Steps A and B), of product as a solid.

後処理

  1. customto destroy the excess sodium borohydride
  2. additionThe reaction mixture was poured into water
  3. extractionextracted with ethyl acetate (3×150 ml)
  4. washThe ethyl acetate was washed with saturated aqueous sodium chloride (150 ml)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationAfter filtration the solvent
  7. customwas removed under reduced pressure
  8. customto yield 5.5 gms (54%, over Steps A and B)

出典と根拠

ORDレコード
ord-be04bfdb20004457acb2cd6e96904541
出典データセット
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04420480

反応ノート

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