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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494104Generated: November 3, 2026

Dimethyl Sulfoxide → Methyl 8-(p-chlorophenylsulfonamido)-4-(formylmethyl)octanoate

https://huagongshe.com/reaction/1494104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl 8-(p-chlorophenylsulfonamido)-4-(2-hydroxyethyl)octanoateHCID 10069054—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductMethyl 8-(p-chlorophenylsulfonamido)-4-(formylmethyl)octanoateHCID 10340312—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 0.47 mL dimethylsulfoxide in 19 mL methylene chloride is cooled to -70° C. and 0.41 mL oxalyl chloride is added slowly. The solution is stirred at -70° C. for 15 minutes and a solution of 0.38 g of methyl 8-(p-chlorophenylsulfonamido)-4-(2-hydroxyethyl)octanoate in 1 mL methylene chloride is added slowly. The solution is stirred at -60° C. for 15 minutes and 1.9 mL triethylamine is added. The mixture is allowed to warm up to room temperature, washed with saturated sodium bicarbonate solution, and the organic phase is dried, filtered and evaporated to obtain a yellow oil. This oil is taken up in ether and washed with saturated sodium bicarbonate solution. The ether layer is dried, filtered and evaporated to yield methyl 8-(p-chlorophenylsulfonamido)4-(formylmethyl)-octanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-957efb7350204eeda3b9a33436f08861
Source noteuspto-grants-1991_06