Vinyl hexanoate → (2R)-2-t-Butoxycarbonylamino-2-ethyl-3-n-hexanoyloxy-1-propanol

HRID 604552

反応式

HRID 604552 の反応式
[C:1]([O:5][C:6]([NH:8][C:9]([CH2:14][CH3:15])([CH2:12][OH:13])[CH2:10][OH:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].[C:16](OC=C)(=[O:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]>C(OC(C)C)(C)C>[C:1]([O:5][C:6]([NH:8][C@@:9]([CH2:14][CH3:15])([CH2:10][O:11][C:16](=[O:22])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH2:12][OH:13])=[O:7])([CH3:4])([CH3:3])[CH3:2]

参加物

4

反応物 2

HCID 76451Vinyl hexanoateHCID 222796962-t-Butoxycarbonylamino-2-ethylpropane-1,3-diol

生成物 1

HCID 86596707(2R)-2-t-Butoxycarbonylamino-2-ethyl-3-n-hexanoyloxy-1-propanol収率 87.3%

試薬・触媒・溶媒 1

HCID 7914Diisopropyl Ether溶媒

実験手順

2-t-Butoxycarbonylamino-2-ethylpropane-1,3-diol (52.9 g, 241 mmol) was suspended in isopropyl ether (1.0 L) and vinyl hexanoate (41.0 mL, 254 mmol) and lipase [Immobilized lipase from Pseudomonas sp., manufactured by TOYOBO Limited, 0.67 U/mg] (2.1 g) was added thereto, followed by stirring of the mixture at room temperature for 4 hours. After the reaction mixture was filtered, the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate, 7:1-4:1-2:1) to obtain the title compound (66.8 g, yield: 87%).

後処理

  1. filtrationAfter the reaction mixture was filtered
  2. customthe filtrate was evaporated under reduced pressure
  3. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate, 7:1-4:1-2:1)

出典と根拠

ORDレコード
ord-64ecbf30adcb4c4098fb7d4af3275ec4
出典データセット
uspto-grants-2011_03
特許番号
US07910617B2

関連ノート

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