Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170772Generated: October 30, 2026

Triethylamine → Methyl 4-formylcyclohexane-1-carboxylate

https://huagongshe.com/reaction/2170772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfur trioxide-pyridineHCID 168533—
ReactantHCID 178501147HCID 178501147—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-formylcyclohexane-1-carboxylateHCID 11252253—

Reaction Steps

The title intermediate (700 mg, 1.87 mmol, 40%) was obtained as a white solid from 4-formyl-cyclohexanecarboxylic acid methyl ester (800 mg, 4.7 mmol) and 4-iodoaniline (601 mg, 2.74 mmol) analogously to Intermediate 75.7. HPLC: GtRet=7.874 min; LC-MS: m/z 374.2 [M+H]+. 4-Formyl-cyclohexanecarboxylic acid methyl ester was prepared by the following method. To a solution of trans-4-hydroxymethyl-cyclohexanecarboxylic acid methyl ester (which is reported in Synthesis Comm. (1982) page 42-43) (861 mg, 5.0 mmol) and Et3N (2.1 mL, 15.0 mmol) in DCM (16 mL) was slowly added a solution of pyridine sulfur trioxide (2.39 g, 15 mmol) in DMSO (10 mL) at 0° C. (ice bath). After 70 min stirring, it was then diluted into DCM and washed with water. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. This crude material (0.8 g, 4.7 mmol) was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051279B2
Source datasetuspto-grants-2015_06
ORD IDord-fb79e48e097f4750b8dff6e1b8ef3114
Source noteuspto-grants-2015_06