戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1906986作成日:2026年10月27日

N-methyl-2-pyrrolidone → 3-Hydroxy-alpha-methyl-L-tyrosine 1-(2,2-dimethyl-1-oxopropoxy)ethyl ester

https://huagongshe.com/reaction/1906986

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物MethyldopaHCID 38853—
反応物Lithium BromideHCID 82050—
反応物1-Chloroethyl pivalateHCID 3016174—
溶媒Ethyl AcetateHCID 8857—
生成物3-Hydroxy-alpha-methyl-L-tyrosine 1-(2,2-dimethyl-1-oxopropoxy)ethyl esterHCID 88126—

反応条件

温度25 °C

反応手順

10 grams (0.047 mole) of α-methyldopa, 4.7 grams of powdered 4A molecular sieves, 6.1 grams (0.070 mole) of lithium bromide and 47 milliliters of N-methylpyrrolidinone were stirred for about one hour at 25° C. To this mixture, 8.1 grams (0.049 mole) of α-chloroethyl pivalate was added and the mixture was aged at 55° C. for 8 hours. At the end of this time, the mixture was cooled to 25° C., diluted with 100 milliliters of ethyl acetate and washed successively with one 200 milliliter and two 100 milliliter portions of saturated sodium bicarbonate solution. The combined sodium bicarbonate washes were extracted with two 100 milliliter portions of ethyl acetate and the combined ethyl acetate extracts concentrated under vacuum to 150 milliliters. The assay yield of α-pivaloyloxyethyl (S)-3-(3,4-dihydroxyphenyl)-2-methylalaninate was found to be 14.4 grams or 90 percent of theoretical.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04654433
出典データセットuspto-grants-1987_03
ORD IDord-e6e58058f4af4af3a05bd51fad74b2f4
出典メモuspto-grants-1987_03