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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370779Generated: October 30, 2026

Ethanesulfonyl chloride → HCID 18512117, compound

https://huagongshe.com/reaction/1370779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 86586222HCID 86586222—
SolventPyridineHCID 1049—
ProductHCID 18512117HCID 18512117—

Reaction Steps

The product from Example 2B (0.03 g, 0.1 mmoles) in pyridine (2 mL) at 0° C. was treated with ethanesulfonyl chloride (0.01 g, 0.12 mmoles). The reaction mixture was quenched after 1 hour with water (2 mL), extracted with diethyl ether (5 mL), washed with water (2×2 mL), rinsed with brine (2 mL), dried (Na2SO4), filtered, and the filtrate concentrated under reduced pressure. The residue was purified by preparative HPLC (CH3CN:0.1% TFA in H2O) on a YMC ODS Guardpak column to provide the title compound. 1H NMR (500 MHz, DMSO-d6) δ1.22 (t, 3H, J=7.3 Hz), 2.40 (s, 3H), 3.02 (dd, 2H, J=14.6, 7.5 Hz), 4.05 (s, 4H), 6.94 (m, 2H), 7.01 (m, 1H), 7.20 (m, 2H), 7.27 (m, 7H), 8.92 (s, 1H); MS (APCI+) m/z 395 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583180B2
Source datasetuspto-grants-2003_06
ORD IDord-99c06899de2a43349fe19ec15e4f17c6
Source noteuspto-grants-2003_06