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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12190생성일: 2026년 10월 25일

Tributylstannane → 4-Benzyl-6,6-dimethyl-morpholine-3-carboxylic acid benzyl ester

https://huagongshe.com/reaction/12190

반응식

참여 물질

역할이름HCID투입량
반응물TributylstannaneHCID 5948—
반응물AzobisisobutyronitrileHCID 6547—
반응물4-Benzyl-6-iodomethyl-6-methyl-morpholine-3-carboxylic acid benzyl esterHCID 67166523—
용매TolueneHCID 1140—
생성물4-Benzyl-6,6-dimethyl-morpholine-3-carboxylic acid benzyl esterHCID 6716576685%

반응 단계

To a solution of 4-benzyl-6-iodomethyl-6-methyl-morpholine-3-carboxylic acid benzyl ester (Intermediate 17, 1.23 g) and tributyltin hydride (1.8 ml, 2.5 eq.) in 11 ml of toluene under gentle reflux was added over 1.5 hr a solution of AIBN in toluene (25 mg/1 ml). The mixture was allowed to cool down and was concentrated to dryness. The residue was partitioned into 15% 1M HCl in acetonitrile and hexane. The separated hexane phase was extracted two times with the acetonitrile solution. The combined acetonitrile solutions were washed with hexane two times and concentrated. The residue was partitioned into ether and 1M K2CO3. The separated ether phase was washed successively with 0.4M Na2S2O3 and brine, dried over MgSO4 and concentrated. The residue was purified on silica (7.5% EtOAc/hexane) to give 760 mg (oil, 85% yield) of compound 4-benzyl-6,6-dimethyl-morpholine-3-carboxylic acid benzyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727985B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-de82173cc7804e4cae31af4e4fc9d489
출처 메모uspto-grants-2010_06