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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426645Generated: November 1, 2026

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

https://huagongshe.com/reaction/1426645

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 mL, 5.38 mmol) in DCM (30.0 mL) at −78° C. was added DMSO (637 mL, 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): δ 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 numberUS08933086B2
Source datasetuspto-grants-2015_01
ORD IDord-8f43301c6b834a2aad35dfb454c9d9df
Source noteuspto-grants-2015_01