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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70134Generated: October 29, 2026

Dimethyl Sulfoxide → 216228-85-2

https://huagongshe.com/reaction/70134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantDi-tert-butyl 2-(hydroxymethyl)piperazine-1,4-dicarboxylateHCID 22711445—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product216228-85-2HCID 2271090280%

Reaction Steps

A solution of DMSO (0.54 mL, 7.66 mmol) in CH2Cl2 (1 mL) was added to a solution of oxalyl chloride (0.33 mL, 3.8 mmol) in CH2Cl2 (8 mL) at −60° C. After 5 min, a solution of di-tert-butyl 2-(hydroxymethyl)piperazine-1,4-dicarboxylate (1.10 g, 3.48 mmol) in CH2Cl2 (3 mL) was added. After 15 min, triethylamine (2.4 mL, 17 mmol) was added, and the reaction mixture was allowed to warm to rt. After 1 h, water (25 mL) was added, the organics were separated, and the aqueous layer was extracted with CH2Cl2 (3×25 mL). The combined organics were washed with brine (3×50 mL), 1% HCl (3×50 mL), water (50 mL), and 5% NaHCO3 (3×50 mL). The organics were dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was purified by column chromatography (10 to 20% EtOAc in Hexanes gradient), yielding 0.873 g (80%) of the desired product as a white solid. Rf=0.70 in 50% EtOAc/Hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822472B2
Source datasetuspto-grants-2014_09
ORD IDord-e68e566e8b764a62968ba5c12cbfd54d
Source noteuspto-grants-2014_09