Benzyl chloroformate → HCID 20681205、化合物

HRID 1693091

反応式

HRID 1693091 の反応式
[CH3:1][C:2]([C:9]([OH:11])=[O:10])([CH2:4][CH2:5][C:6]([OH:8])=[O:7])[NH2:3].Cl[C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14]>[OH-].[Na+]>[CH2:16]([O:15][C:13]([NH:3][C@:2]([CH3:1])([C:9]([OH:11])=[O:10])[CH2:4][CH2:5][C:6]([OH:8])=[O:7])=[O:14])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

参加物

4

実験手順

To a stirred solution of α-methyl-D,L-glutamic acid (10 g, 62 mmol) in 2 N sodium hydroxide (62 mL) at 0-5° C. was added benzyl chloroformate (12.7 g, 74.4 mmol) over 30 min. After the addition was complete the reaction mixture was stirred at room temperature for 3 hours. During this time the pH was maintained at 11 by addition of 2N sodium hydroxide (33 mL). The reaction mixture was then extracted with ether (60 mL). The aqueous layer was cooled in an ice bath and then acidified with 4N hydrochloric acid (34 mL) to pH=1. The resulting mixture was extracted with ethyl acetate (3×100 mL). The combined ethyl acetate extracts were washed with brine (60 mL) and dried (MgSO4). The solvent was removed in vacuo to give 15.2 g (83%) of N-benzyloxycarbonyl-α-methylglutamic acid as an oil: 1H NMR (CDCl3) δ 8.73(m, 5H), 5.77(b, 1H), 5.09(s, 2H), 2.45-2.27(m, 4H), 2.0(s, 3H).

後処理

  1. additionAfter the addition
  2. extractionThe reaction mixture was then extracted with ether (60 mL)
  3. temperatureThe aqueous layer was cooled in an ice bath
  4. extractionThe resulting mixture was extracted with ethyl acetate (3×100 mL)
  5. washThe combined ethyl acetate extracts were washed with brine (60 mL)
  6. dry with materialdried (MgSO4)
  7. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-34899f07dc884adb81f157316b9b3898
出典データセット
uspto-grants-2012_04
特許番号
US08158653B2

関連ノート

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