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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25589Generated: October 30, 2026

Carbon Dioxide → tert-butyl N-methyl-N-[trans-4-formylcyclohexyl]carbamate

https://huagongshe.com/reaction/25589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178486045HCID 178486045—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-methyl-N-[trans-4-formylcyclohexyl]carbamateHCID 86584984100.4%

Reaction Steps

To a dry-ice cooled solution of 8.94 ml (125.9 mmol) DMSO in 150 ml CH2Cl2 was added 5.95 ml (69.24 mmol) oxalylchloride. After 5 min at −78° C., a solution of 16.2 g (66.5 mmol) trans-(4-Hydroxymethyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester in 50 ml of CH2Cl2, was added slowly. 10 min later, 43.8 ml (314.75 mmol) of Et3N was added, and the mixture was allowed to attain RT. The mixture was partitioned between Et2O/1N HCl and water. The solvent was evaporated under reduced pressure yielding 16.12 g of clean (4-Formyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester, MS: 241 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858651B2
Source datasetuspto-grants-2005_02
ORD IDord-09d10b739a05479196e4a9098b444134
Source noteuspto-grants-2005_02