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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245058Generated: November 2, 2026

Dimethyl Sulfoxide → tert-butyl N-(4-oxooxolan-3-yl)carbamate

https://huagongshe.com/reaction/245058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttrans-tert-butyl 4-hydroxytetrahydrofuran-3-ylcarbaMateHCID 91663897—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-(4-oxooxolan-3-yl)carbamateHCID 7143757244.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of oxalyl chloride (3.20 mL, 36.9 mmol) in THF (137 mL) is cooled to −78° C. under nitrogen and treated dropwise with DMSO (5.24 mL, 73.8 mmol). The mixture is stirred for 20 min at −78° C., whereupon trans-tert-butyl N-[4-hydroxytetrahydrofuran-3-yl]carbamate (5.00 g, 24.6 mmol) is added. Stirring at −78° C. is continued for 1 h. Triethylamine (18.5 mL, 133 mmol) is added and the reaction is warmed to room temperature. The reaction is stirred for 16 h, then water (100 mL) is added and the reaction is concentrated in vacuo to remove THF. The mixture is extracted with EtOAc (3×70 mL), the combined organics dried over magnesium sulfate, filtered, and concentrated to give 6.4 g of crude product as an orange oil. The crude product is purified on silica gel (220 g, 15-30% EtOAc/hexanes) to give the title compound as a yellow oil (2.20 g, 44%). GC-MS m/z 201 (M)+, 143 (M-t-Bu)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658693B2
Source datasetuspto-grants-2014_02
ORD IDord-f6566f26513948fea0a7289b83e288aa
Source noteuspto-grants-2014_02