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Water → (2S,5R)-2-(4-chlorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

HRID 1677073
ノート
印刷プレビュー

反応式

HRID 1677073 の反応式
O1CCCC1.C([O:8][C:9](=O)[C@H:10]([NH:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:11][CH2:12][C:13]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1)=O)C.O>C(OCC)(=O)C>[C:26]([O:25][C:23]([N:22]1[C@@H:10]([CH2:9][OH:8])[CH2:11][CH2:12][C@H:13]1[C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1)=[O:24])([CH3:29])([CH3:28])[CH3:27]
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 962WaterHCID 8028TetrahydrofuranHCID 67371186ethyl (R)-2-tert-butoxycarbonylamino-5-(4-chlorophenyl)-5-oxopentanoate

生成物 1

HCID 67375406(2S,5R)-2-(4-chlorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester収率 104.4%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

Ice-cold lithium borohydride (277 mg) was added to a tetrahydrofuran (40 mL) solution of (2R,5S)-5-(4-chlorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester (3 g) obtained in Example 8. Stirring was continued for 30 minutes at the same temperature and for 13 hours at room temperature. Water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine and was dried over anhydrous magnesium sulfate. The solvent was removed under a vacuum, and the title compound (2.64 g) was obtained. The physical property values are as follows.

後処理

  1. customthe organic layer was partitioned
  2. washThe organic layer was washed with brine
  3. dry with materialwas dried over anhydrous magnesium sulfate
  4. customThe solvent was removed under a vacuum

出典と根拠

ORDレコード
ord-091702770f6f4cf980bbafe4dc6f797a
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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このページの内容参加物実験手順後処理出典と根拠反応ノート