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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085370Generated: October 31, 2026

Dimethyl Sulfoxide → 2-Oxazolecarboxaldehyde, 5-(1,1-dimethylethyl)- (9CI)

https://huagongshe.com/reaction/2085370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(1,1-Dimethylethyl)-2-oxazolemethanolHCID 22731089—
SolventDichloromethaneHCID 6344—
Product2-Oxazolecarboxaldehyde, 5-(1,1-dimethylethyl)- (9CI)HCID 2273108687.8%

Reaction Steps

To a stirred solution of oxalyl chloride (45 mL, 90 mmole) at −78 deg C. under argon was added dropwise dimethyl sulfoxide (8.80 mL, 124 mmole). The reaction mixture was stirred at −78 deg C. for 10 min., and was treated with a solution of 2-hydroxymethyl-5-t-butyloxazole (11.7 g, 75.1 mmole) in anhydrous methylene chloride (30 mL) over 20 min. The mixture was stirred at this temperature for 1 hour, then triethylamine was added slowly (31.0 mL, 222 mmole), during which the reaction mixture became a yellowish slurry. After stirring at −78 deg C. for 20 min, the reaction mixture was warmed to room temperature, added with methylene chloride (100 mL) and stirred for 1 hour. The solid was filtered off and washed with EtOAc. The filtrate was washed with 5% aqueous citric acid (100 mL) and brine (50 mL), dried over MgSO4. Concentration and column chromatography (silica gel, EtOAc/hexane 1:4) afforded 2-formyl-5-t-butyloxazole as a light yellow oil (10.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720347B2
Source datasetuspto-grants-2004_04
ORD IDord-0458d115ed824ba6a04dd551ade56c9f
Source noteuspto-grants-2004_04