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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032903Generated: October 31, 2026

Triethylamine → HCID 22381912, compound

https://huagongshe.com/reaction/1032903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantCyclobutylcarbinolHCID 78130—
SolventDiethyl EtherHCID 3283—
ProductHCID 22381912HCID 22381912103.4%

Reaction Steps

Cyclobutanemethanol (24.9 g; 0.287 mol) and methanesulfonyl chloride (35.3 g; 0.302 mol) in dry ether (250 ml) was cooled to -20° C. under dry nitrogen. Triethylamine (44 ml; 0.32 mol) was added dropwise over 15 min with external cooling so that the reaction temperature remained below -5° C. The reaction mixture was allowed to warm to room temperature over 1 h and then filtered. The remaining solid was washed with ether. The ether solutions were combined and the ether evaporated, to afford crude cyclobutylmethyl methanesulfonate (48.75 g) as a pale yellow liquid, which was used in the next step without further purification. NMR - d(CDCl3 ; 60 MHz) 1.6-2.9 (7H, m), 3.0 (3H, s) and 4.1 (2H, d, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308830
Source datasetuspto-grants-1994_05
ORD IDord-78572052a87842bdaea973ef1123dcfb
Source noteuspto-grants-1994_05