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Iodine → 2-Methoxy-pyrrolidine-1-carboxylic acid benzyl ester

HRID 132819
ノート
印刷プレビュー

反応式

HRID 132819 の反応式
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][C@H:12]1C(O)=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19](OC1C(OC(=O)C)=C(I=O)C=CC=1)(=[O:21])C.II.CO>ClCCl>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[O:21][CH3:19])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 807IodineHCID 887MethanolHCID 101987Benzyloxycarbonyl-L-prolineHCID 21113495Diacetoxyiodosobenzene

生成物 1

HCID 109224852-Methoxy-pyrrolidine-1-carboxylic acid benzyl ester収率 88.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a mixture of (S)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (purchased at Fluka, Ref 97090, 6 g, 1.0 eq.) in dichloromethane (300 mL) was added diacetoxyiodosobenzene (15.8 g, 2 eq.) and iodine (3.0 eq., 0.5 eq.). The mixture was stirred 5 h at room temperature. Methanol (12 mL) was added and the reaction mixture was stirred for an additional 1.5 h at room temperature, partitioned between an aqueous solution of sodium sulfite and dichloromethane. The organic layer was washed with an aqueous solution of sodium sulfite, brine, evaporated in vacuo and purified on silica eluting with 9:1 cyclohexane/ethyl acetate to yield 5.0 g (88%) of the desired product as light yellow oil. MS (m/e): 235.5 (MH+, 100%)

後処理

  1. stirringthe reaction mixture was stirred for an additional 1.5 h at room temperature
  2. custompartitioned between an aqueous solution of sodium sulfite and dichloromethane
  3. washThe organic layer was washed with an aqueous solution of sodium sulfite, brine
  4. customevaporated in vacuo
  5. custompurified on silica eluting with 9:1 cyclohexane/ethyl acetate

出典と根拠

ORDレコード
ord-b86cbbeb5da042a2aaf26fadcae3ef6d
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07388095B2

反応ノート

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