244205-60-5 → 1-Amino-2-phenylcyclopropane-1-carboxylic acid
反応式
C(OC([NH:8][C@:9]1([C:18]([OH:20])=[O:19])[CH2:11][C@H:10]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=O)(C)(C)C.Cl.O1CCOCC1>C(OCC)C>[NH2:8][C@@:9]1([C:18]([OH:20])=[O:19])[CH2:11][C@@H:10]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
4
実験手順
To commercially available (1R,2S)-1-tert-butoxycarbonylamino-2-phenylcyclopropanecarboxylic acid (130 mg, 0.45 mmol) was added 4N hydrochloric acid—1,4-dioxane solution (2.0 mL, 16 v/w) and the mixture was stirred for 1 hr at room temperature. Diethyl ether (1.0 mL) was added thereto and the mixture was stirred for 5 min, after which the resulting crystals were collected by filtration. The crystals were washed with diethyl ether (1.0 mL) and dried under reduced pressure to give the title compound (81 mg, white powder, yield 84%).
後処理
- stirringthe mixture was stirred for 5 min
- filtrationafter which the resulting crystals were collected by filtration
- washThe crystals were washed with diethyl ether (1.0 mL)
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-afd4e59a7c8a428b82db1d71553f88a6
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351825B2
反応ノート
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