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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968525Generated: October 26, 2026

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

https://huagongshe.com/reaction/968525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylprop-2-En-1-OlHCID 308—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acidHCID 69415969—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid (3-phenyl)-allyl esterHCID 8659860050.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304057B2
Source datasetuspto-grants-2007_12
ORD IDord-f96ecf96c8cf4e4da5d0ba479f24478d
Source noteuspto-grants-2007_12