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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710408Generated: November 3, 2026

Triethylamine → HCID 23631899, compound

https://huagongshe.com/reaction/1710408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(5-Bromopyridin-2-yl)methanolHCID 5200169—
SolventDichloromethaneHCID 6344—
ProductHCID 23631899HCID 23631899—

Reaction Steps

A mixture of (5-Bromo-pyridin-2-yl)-methanol (60 mg, 0.32 mmol) in dichloromethane (2 ml) was cooled in as ice bath. To the mixture was then added triethylamine (0.13 mL, 0.96 mmol) followed by methanesulfonyl chloride (0.05 mL, 0.64 mmol). The reaction mixture was stirred at room temperature for 2 hours. To the reaction mixture was added saturated aqueous sodium bicarbonate (5 mL). The organic phase was separated and the aqueous phase extracted further with dichloromethane (2×5 mL). The combined organic phase was washed with brine, dried over sodium sulfate and concentrated to give the product as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790717B2
Source datasetuspto-grants-2010_09
ORD IDord-323ce718afd2492f832c027d548a72a0
Source noteuspto-grants-2010_09