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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355549Generated: October 30, 2026

Triethylamine → HCID 10503096, compound

https://huagongshe.com/reaction/355549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10808359HCID 10808359—
SolventDichloromethaneHCID 6344—
ProductHCID 10503096HCID 1050309694.2%

Reaction Steps

To a stirred, ice-cold solution of 23.19 g (64.68 mmol) of the alcohol (16) and 13.5 ml (96.86 mmol) of triethylamine in 200 ml of CH2Cl2 was added 6.0 ml (77.52 mmol) of methanesulfonyl chloride. After 30 minutes at 0° C., the reaction mixture was warmed to room temperature. After another 30 minutes, the reaction mixture was diluted with CH2Cl2 and then washed sequentially with 0.5N HCl, saturated NaHCO3 and saturated NaCl. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure, yielding 26.61 g (94%) of the desired mesylate (17) as a colorless oil, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05831100
Source datasetuspto-grants-1998_11
ORD IDord-4ad7509896d844b2a9ea2af72633fba8
Source noteuspto-grants-1998_11