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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968525생성일: 2026년 10월 26일

3-Phenylprop-2-En-1-Ol → (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid (3-phenyl)-allyl ester

https://huagongshe.com/reaction/968525

반응식

참여 물질

역할이름HCID투입량
반응물3-Phenylprop-2-En-1-OlHCID 308—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acidHCID 69415969—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid (3-phenyl)-allyl esterHCID 8659860050.3%

반응 단계

0.301 g (1 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.200 g (1.5 mmol) of (3-phenyl)-allyl alcohol, 0.088 g (0.33 mmol) of CAS, 0.227 g (1.2 mmol) of DCC and 0.04 g (0.33 mmol) of DMAP were dissolved in 15 mL of CH2Cl2. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: ethyl acetate:cyclohexane=1:4) to obtain the product as a oil (0.21 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07304057B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-f96ecf96c8cf4e4da5d0ba479f24478d
출처 메모uspto-grants-2007_12