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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968875Generated: October 29, 2026

Dimethyl Sulfoxide → (4-Formyltetrahydropyran-4-yl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1968875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-butyl N-[4-(hydroxymethyl)oxan-4-yl]carbamateHCID 67114425—
SolventDichloromethaneHCID 6344—
Product(4-Formyltetrahydropyran-4-yl)carbamic acid tert-butyl esterHCID 5971879392.6%

Reaction Conditions

Temperature-65 °C

Reaction Steps

Anhydrous dimethyl sulfoxide (3.0 mL, 42.2 mmol) was added to a −65° C. solution of oxalyl chloride (2.0 mL, 22.9 mmol) in anhydrous dichloromethane (100 mL) and allowed to stir at −65° C. under N2 blanket for 3 minutes, after which time a solution of (4-hydroxymethyl-tetrahydro-pyran-4-yl)-carbamic acid tert-butyl ester (4.89 g, 21.1 mmol) in anhydrous dichloromethane (25 mL) was added. When 25 minutes had elapsed, triethylamine (14.7 mL, 105.5 mmol) was added and the reaction solution allowed to stir for a further 20 minutes at −65° C.; then the cold bath was removed and the reaction warmed to ambient temperature, washed with saturated aqueous sodium chloride (500 mL), dried (MgSO4), and evaporated to afford 4.48 g of clear yellow viscous liquid which was used without further purification. LRMS (ESI) m/z 230.2 [(M+H)+, calcd for C11H20NO4230.3].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426414B2
Source datasetuspto-grants-2013_04
ORD IDord-1d7bfe9c73174aaabb4bedb2747d1029
Source noteuspto-grants-2013_04