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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356985Generated: October 31, 2026

Triethylamine → HCID 58668690, compound

https://huagongshe.com/reaction/2356985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68459038HCID 68459038—
SolventDichloromethaneHCID 6344—
ProductHCID 58668690HCID 58668690—

Reaction Steps

A solution of 2-[7-(3-Fluoro-benzenesulfonyl)-chroman-4-yl]-ethanol (1.35 g, 4.01 mmol) in CH2Cl2 (40 ml) was cooled to 0° C. Et3N (4.06 g, 40.2 mmol) was added at 0° C. followed by methanesulfonylchloride (0.91 g, 8.00 mmol). The reaction mixture was stirred in an ice bath for 2 hours, then diluted with CH2Cl2, washed with brine, dried with MgSO4, filtered and concentrated to give AN oil residue. The residue was purified with flash chromatography to give methanesulfonic acid 2-[7-(3-fluoro-benzenesulfonyl)-chroman-4-yl]-ethyl ester as a clear oil: 1.35 g; MS: 415.2 (M+H)+, 829.2 (2M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759389B2
Source datasetuspto-grants-2010_07
ORD IDord-8ffc61180c504e75bffe95904e7ca66a
Source noteuspto-grants-2010_07