Methyl chloroformate → Nalpha-methoxycarbonyl-DL-methionine amide
反応式
[CH3:1][O:2][C:3](Cl)=[O:4].[NH2:6][CH:7]([C:12]([NH2:14])=[O:13])[CH2:8][CH2:9][S:10][CH3:11].[OH-].[Na+]>O>[CH3:1][O:2][C:3]([NH:6][CH:7]([C:12]([NH2:14])=[O:13])[CH2:8][CH2:9][S:10][CH3:11])=[O:4]参加物
実験手順
85 ml (1.11 moles) methylchloroformate were dripped into a solution of 150 g (1.02 moles) DL-methionine amide in 200 ml water at 5-10° C., during which the pH was maintained at 8-10 by the addition of sodium hydroxide solution. After 30 min of subsequent reaction, 60 ml water was added, whereupon crystals formed which were filtered off, washed with water and dissolved in 250 ml water. This solution was extracted twice and the crystallization mother liquor extracted once with 500 ml methylene chloride in each instance. After drying in a vacuum, 162 g yellowish, crystalline residue remained. It was dissolved in 200 ml hot ethanol. Then, 400 ml MTBE was added and after the appearance of the first colorless crystals another 200 ml MTBE. After cooling in an ice bath, filtering off, washing with 200 ml MTBE and drying, 127 g (60k) Nα-methoxycarbonyl-DL-methionine amide with a melting point of 93-94° C. was obtained.
後処理
- additionwas added, whereupon crystals
- customformed which
- filtrationwere filtered off
- washwashed with water
- dissolutiondissolved in 250 ml water
- extractionThis solution was extracted twice
- extractionthe crystallization mother liquor extracted once with 500 ml methylene chloride in each instance
- customAfter drying in a vacuum, 162 g yellowish
- dissolutionIt was dissolved in 200 ml hot ethanol
- additionThen, 400 ml MTBE was added
- temperatureAfter cooling in an ice bath
- filtrationfiltering off
- washwashing with 200 ml MTBE
- customdrying
出典と根拠
- ORDレコード
- ord-7dd267102c25483d9307fdc0a30a3531
- 出典データセット
- uspto-grants-2001_12
- 特許番号
- US06333176B1
反応ノート
読み込み中…