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HRID 12190作成日:2026年10月26日

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

https://huagongshe.com/reaction/12190

反応式

関与物質

役割名称HCID仕込み量
反応物TributylstannaneHCID 5948—
反応物AzobisisobutyronitrileHCID 6547—
反応物4-Benzyl-6-iodomethyl-6-methyl-morpholine-3-carboxylic acid benzyl esterHCID 67166523—
溶媒TolueneHCID 1140—
生成物4-Benzyl-6,6-dimethyl-morpholine-3-carboxylic acid benzyl esterHCID 6716576685%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727985B2
出典データセットuspto-grants-2010_06
ORD IDord-de82173cc7804e4cae31af4e4fc9d489
出典メモuspto-grants-2010_06