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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038484Generated: October 30, 2026

4-Toluenesulfonyl chloride → 3-Cyclopropylprop-2-ynyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/2038484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant3-Cyclopropylprop-2-yn-1-olHCID 2793757—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-Cyclopropylprop-2-ynyl 4-methylbenzenesulfonateHCID 57684700—

Reaction Steps

To a stirred solution of crude 3-cyclopropylprop-2-yn-1-ol (intermediate AT) (0.55 mg) in 10 mL of CH2Cl2 was added TsCl (1.33 g, 6.87 mmol) and DMAP (0.035 g, 0.2865 mmol) at 0° C. Triethylamine (0.96 mL, 6.87 mmol) was added dropwise to the mixture and the reaction temperature was held so as not to exceed 0° C. After stirring for 3 h, the mixture was quenched with 10 mL of water. The aqueous layer was extracted twice with 20 mL each of CH2Cl2. The organic layer was washed with 20% HCl and water prior to drying over anhydrous Na2SO4. The organic phase was concentrated and the crude product was purified by gel column chromatography to obtain intermediate AU (0.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575321B2
Source datasetuspto-grants-2013_11
ORD IDord-55d05407dc9944c6b35c559fa04a65b9
Source noteuspto-grants-2013_11