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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962817Generated: October 31, 2026

Dimethyl Sulfoxide → tert-butyl N-((1-formylcyclopentyl)methyl)carbamate

https://huagongshe.com/reaction/1962817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamateHCID 57478044—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-((1-formylcyclopentyl)methyl)carbamateHCID 5748069194%

Reaction Steps

To a solution of oxalyl chloride (456 μL, 5.38 mmol) in DCM (30.0 mL) at −78° C. was added DMSO (637 μL, 8.97 mmol) and the resulting mixture was stirred for 5 minutes. tert-Butyl [1-(hydroxymethyl)cyclopentyl]methylcarbamate (1.03 g, 4.48 mmol) in DCM (10.0 mL) was added and the resulting mixture was stirred for 30 minutes at −78° C. TEA (2.50 mL, 17.9 mmol) was added and the resulting mixture was allowed to warm to ambient temperature over 30 minutes. Water was added. The organic phase was washed sequentially with 0.1 N HCl, water, saturated sodium bicarbonate solution, and brine, and then dried over sodium sulfate and the solvent was removed in vacuo to afford the product (957 mg, 94%). 1H NMR (300 MHz, CDCl3): 9.39 (s, 1H), 4.94 (br s, 1H), 3.25 (d, 2H), 1.89-1.46 (m, 8H), 1.41 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415362B2
Source datasetuspto-grants-2013_04
ORD IDord-229a7203498d477d960c79f1dfc3adcc
Source noteuspto-grants-2013_04