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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487371생성일: 2026년 10월 24일

Hydrochloric Acid → N-Benzoyl-3-phenylisoserine, (2R,3S)-

https://huagongshe.com/ko/reaction/487371

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzoyl chlorideHCID 7412—
반응물Sodium BicarbonateHCID 516892—
반응물3-Phenylisoserine, (2R,3S)-HCID 7020763—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-Benzoyl-3-phenylisoserine, (2R,3S)-HCID 276228972%

반응 단계

To a solution of compound 5.HCl (219 mg, 1.00 mmol) in water (10 mL) containing sodium bicarbonate (500 mg, 5.95 mmol) was added a solution of benzoyl chloride (0.14 mL, 1.20 mmol) in dichloromethane (5.0 mL). The mixture was vigorously stirred for 16 h at room temperature. The reaction mixture was acidified with 0.1N HCl and the crude product was extracted with ethyl acetate (40 mL×3). The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo to dryness. The residue was purified on a short silica gel column using chloroform/methanol (2/1) as the eluant to give N-benzoyl-(2R,3S)-3-phenylisoserine (6) (205 mg, 72%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294737
출처 데이터셋uspto-grants-1994_03
ORD IDord-01d7f9b6a7c348acb29c19cf0c535ecb
출처 메모uspto-grants-1994_03