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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266714생성일: 2026년 10월 27일

Hydrochloric Acid → (Benzyloxy)acetic acid

https://huagongshe.com/reaction/266714

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물EperezolidHCID 73214—
반응물Benzyloxyacetyl chlorideHCID 177085—
용매DichloromethaneHCID 6344—
생성물(Benzyloxy)acetic acidHCID 29030144%

반응 단계

To a mixture of 200 mg (0.508 mmol) of U-100592 (Ex. 1), 149 mg (1.47 mmol, 0.205 mL), and 5 mL methylene chloride at 0° C. benzyloxyacetylchloride was added dropwise. The reaction was allowed to warm slowly up to room temperature. After stirring for 5 hours, 5 mL of 1N HCl was added, and the resulting layers were separated. The aqueous layer was extracted with methylene chloride (3×5 mL). The combined organic layers were washed with brine and dried (MgSO4) then filtered and concentrated to a white solid. The crude was dissolved in a small amount of methylene chloride and methanol and was placed on a 22 cm×2.5 cm 40-60 μ silica column. The column was eluted with ethyl acetate, 2% methanol/ethylacetate, 4% methanol/ethyl acetate, 6% methanol/ethyl acetate, 8% methanol/ethyl acetate, and 10% methanol/ethyl acetate (250 mL each). The appropriate fractions were pooled to provide 120 mg (44%) of benzyloxyacetic acid, 2-[-[4-[5-(acetylamino)methyl]-2-oxo-3-oxazolidinyl]-2-fluorophenyl]-1-piperazinyl]-2-oxoethyl ester, (S)-; as a white solid (mp=146°-148° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05652238
출처 데이터셋uspto-grants-1997_07
ORD IDord-bd3e002bf3634c5583656059f75eaef5
출처 메모uspto-grants-1997_07