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Sodium Methoxide → (S)-1-[(3R,5R)-5-(4-chlorophenyl)morpholine-3-yl]ethanol

HRID 1677066
ノート
印刷プレビュー

反応式

HRID 1677066 の反応式
C[O-].[Na+].[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([C@H:11]2[NH:16][C@@H:15]([C@@H:17]([O:19]C(=O)C3C=CC([N+]([O-])=O)=CC=3)[CH3:18])[CH2:14][O:13][CH2:12]2)=[CH:7][CH:6]=1>CO>[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([C@H:11]2[NH:16][C@@H:15]([C@@H:17]([OH:19])[CH3:18])[CH2:14][O:13][CH2:12]2)=[CH:9][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10942334Sodium MethoxideHCID 673717534-nitrobenzoic acid (S)-1-[(3R,5R)-5-(4-chlorophenyl)morpholin-3-yl]ethyl ester

生成物 1

HCID 68716014(S)-1-[(3R,5R)-5-(4-chlorophenyl)morpholine-3-yl]ethanol収率 92.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Sodium methoxide (1.9 mL, 28% methanol solution) was added to a methanol (40 mL) solution of 4-nitrobenzoic acid (S)-1-[(3R,5R)-5-(4-chlorophenyl)morpholin-3 yl]ethyl ester (1.46 g). Stirring was continued for 1 hour at room temperature. The solvent was removed under a vacuum, and ethyl acetate and water were added, and the organic layer was partitioned. The organic layer was washed with brine, and the resultant was dried over anhydrous magnesium sulfate. The solvent was removed under a vacuum, and the residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→1/3), and the title compound (833 mg) was obtained. The physical property values are as follows.

後処理

  1. customThe solvent was removed under a vacuum, and ethyl acetate and water
  2. additionwere added
  3. customthe organic layer was partitioned
  4. washThe organic layer was washed with brine
  5. dry with materialthe resultant was dried over anhydrous magnesium sulfate
  6. customThe solvent was removed under a vacuum
  7. customthe residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→1/3)

出典と根拠

ORDレコード
ord-6224207b89754f37b27a0d81ee674d15
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08008293B2

反応ノート

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