돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248813생성일: 2026년 10월 24일

4-Methylmorpholine → Glycine,n-(1-oxo-3-phenyl-2-propen-1-yl)-, methyl ester

https://huagongshe.com/ko/reaction/248813

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물3-Phenylprop-2-enoyl chlorideHCID 66023—
반응물Glycine methyl ester hydrochlorideHCID 122755—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Glycine,n-(1-oxo-3-phenyl-2-propen-1-yl)-, methyl esterHCID 582979—

반응 단계

Glycine methyl ester hydrochloride was suspended in tetrahydrofuran, the suspension was cooled to -5° C. to -10° C., and then half of the N-methylmorpholine was added. Cinnamoyl chloride was added immediately, followed by the other half of the N-methylmorpholine. The reaction mixture was stirred for 30 minutes at low temperature, then it was allowed to warm to room temperature and stirring was continued for 2 to 3 hours. After being diluted with ethyl acetate (about 750 ml) the solution was washed with water (three times), an aqueous solution of 0.5 N hydrochloric acid (three times) and finally with water. The organic phase was dried over magnesium sulfate, filtered and evaporated to dryness under reduced pressure. The residue was triturated with petroleum ether is order to induce crystallization. The product was left to stand for about 14 hours at 4° C., then it was filtered off and dried in a vacuum. It was used in the next step without further purification. 31 g of product were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212158
출처 데이터셋uspto-grants-1993_05
ORD IDord-4d6ed1c7336c41c6a2513bddea82d243
출처 메모uspto-grants-1993_05