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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515451생성일: 2026년 10월 24일

Hydrochloric Acid → 3-(4-Methoxy-benzylamino)-2-methyl-propan-1-ol

https://huagongshe.com/ko/reaction/515451

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물p-Anisoyl chlorideHCID 7477—
반응물Sodium HydroxideHCID 14798—
반응물Beta-Aminoisobutyric AcidHCID 64956—
용매TetrahydrofuranHCID 8028—
생성물3-(4-Methoxy-benzylamino)-2-methyl-propan-1-olHCID 6152771282%

반응 단계

To a solution of 3-amino-2-methyl-propionic acid (5.00 g, 48.4 mmol) in tetrahydrofuran (107 ml) and 1N sodium hydroxide (107 ml, 107 mmol) was added 4-methoxybenzoyl chloride (8.69 g, 50.9 mmol) at 0° C. The mixture was stirred at room temperature for 3 hours and partitioned between water and ethyl acetate. The water phase was washed with ethyl acetate and acidified with 1N hydrochloric acid. The product was extracted with ethyl acetate. The organic phase was dried over sodium sulfate, and concentrated in vacuo. To the residue dissolved into tetrahydrofuran (20 ml) was added 1M borane-tetrahydrofuran complex (6.40 ml, 6.40 mmol) at 0° C. The mixture was stirred at room temperature. After 30 minutes, the mixture was refluxed for 5 hours and acidified with 3N hydrochloric acid. The acidic aqueous solution was stirred at 60° C. for 2 hours. The organic solvent was evaporated under reduced pressure, then the residue was partitioned between water and ethyl acetate. The water phase was washed with ethyl acetate and basified with 3N sodium hydroxide. The product was extracted with chloroform. The organic phase was dried over sodium sulfate, and concentrated in vacuo to afford 3-(4-methoxy-benzylamino)-2-methyl-propan-1-ol as colorless oil (8.28 g, 82%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108957B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-ac9b9b75e84d454fb8d92ebe3b661c9f
출처 메모uspto-grants-2015_08