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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1805212생성일: 2026년 10월 27일

2,2-Dimethoxypropane → (RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1805212

반응식

참여 물질

역할이름HCID투입량
반응물2,2-DimethoxypropaneHCID 6495—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물n-Boc-[2-hydroxy-1-(4-iodophenyl)ethyl]-amineHCID 67151743—
용매DichloromethaneHCID 6344—
생성물(RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 6715164489%

반응 단계

To a stirred solution of (RS)-[2-hydroxy-1-(4-iodo-phenyl)-ethyl]-carbamic acid tert-butyl ester (7.97 g) in dichloromethane (400 ml) were added sequentially 2,2-dimethoxypropane (36 ml) and p-toluenesulphonic acid monohydrate (0.75 g) and the mixture was stirred at room temperature for 18 hours. The mixture was then washed with 0.5 N aq NaOH, the phases were separated and the organic phase was dried over sodium sulphate, filtered and concentrated in vacuo to afford (RS)-4-(4-iodo-phenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (7.05 g, 89%) as a yellow solid. MS (EI): 403 (M+), 388 ([M-CH3]+), 332 ([M-CH3—C4H8]+), 288 ([M-CH3—C4H8—CO2]+), 57 ([C4H9]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354441B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-b6fdfb1ceb0049eab88a3d6af6ca74b1
출처 메모uspto-grants-2013_01