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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082186Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 15549882, compound

https://huagongshe.com/reaction/1082186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 15549881HCID 15549881—
SolventDichloromethaneHCID 6344—
ProductHCID 15549882HCID 1554988279%

Reaction Steps

Under argon atmosphere, a solution of 4.22 g of methyl (2S,3R)-3-cyclopropyl-2,3-dihydroxypropionate in 140 ml of methylene chloride is cooled to -3° C. Then, 4.00 g of triethylamine and 5.17 g of p-toluenesulfonyl chloride are added to the mixture successively. The mixture is stirred for 3 days. Then, the solvent is removed in vacuo. The residue is poured into a mixture of ethyl acetate and water. The organic layer is washed with brine and dried. The solvent is removed in vacuo. The residue is purified by silica gel column chromatography (solvent; hexane:ethyl acetate=1:3) to give 6.54 g of methyl (2S,3R)-3-cyclopropyl-3-hydroxy-2-(p-toluenesulfonyloxy)propionate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589502
Source datasetuspto-grants-1996_12
ORD IDord-a26324051b854a1b8ff2a33482f40546
Source noteuspto-grants-1996_12