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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906986생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1906986

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참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물MethyldopaHCID 38853—
반응물Lithium BromideHCID 82050—
반응물1-Chloroethyl pivalateHCID 3016174—
용매Ethyl AcetateHCID 8857—
생성물3-Hydroxy-alpha-methyl-L-tyrosine 1-(2,2-dimethyl-1-oxopropoxy)ethyl esterHCID 88126—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04654433
출처 데이터셋uspto-grants-1987_03
ORD IDord-e6e58058f4af4af3a05bd51fad74b2f4
출처 메모uspto-grants-1987_03