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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244536Generated: October 30, 2026

Triethylamine → HCID 86604088, compound

https://huagongshe.com/reaction/244536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 23367041HCID 23367041—
SolventDichloromethaneHCID 6344—
ProductHCID 86604088HCID 8660408891%

Reaction Steps

Octahydro-2H-quinolizin-3-ylmethanol (600 mg, 3.55 mmol) was dissolved in dichloromethane (8 mL) and triethylamine (1.5 mL, 10.8 mmol) was added at 0° C. followed by dropwise addition of methanesulfonyl chloride (0.56 mL, 7.16 mmol). The solution was warmed to room temperature and stirred for 1.25 h and then was concentrated in vacuo. The residue was partitioned between ethyl acetate and saturated sodium bicarbonate solution. The aqueous portion was extracted with ethyl acetate. The combined organic portion was washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford octahydro-2H-quinolizin-3-ylmethyl methanesulfonate as an orange oil (796 mg, 3.22 mmol, 91% yield). MS (EI) for C11H21NO3S: 248 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658654B2
Source datasetuspto-grants-2014_02
ORD IDord-4ec1df18fbd2476fac18c7d3fd21c980
Source noteuspto-grants-2014_02