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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789531Generated: October 30, 2026

Pyridine → HCID 13924083, compound

https://huagongshe.com/reaction/1789531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15053054HCID 15053054—
SolventDimethylformamideHCID 6228—
ProductHCID 13924083HCID 13924083—

Reaction Steps

3-(4-Hydroxybut-1-yl)cyclopentene {2-cyclopentene-1-butanol} (51 g, 0.37 moles) is diluted in dimethylformamide (100 ml) and added to pyridine (38 g, 0.40 moles). The solution is stirred and methanesulfonyl chloride (46 g, 0.40 moles) is added dropwise over 10 minutes. The reaction is partitioned between hexane (500 ml) and the organic phase separated. The aqueous layer is extracted with hexane (2×500 ml) and the organic extracts combined. The solvent volume is reduced under vacuum and the residue dried over anhydrous magnesium sulfate. The solid is filtered off and the remaining solvent removed leaving a clear yellow oil. The crude product is fractionally distilled under reduced pressure leaving a clear, colorless oil (43 g, 0.27 moles), BP 40°0/0.2 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689349
Source datasetuspto-grants-1987_08
ORD IDord-4312836202594ea2b2a1aafcadb9333b
Source noteuspto-grants-1987_08