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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131533Generated: October 31, 2026

Thionyl Chloride → Benzylmethyl-(2-pyridin-3-ylcyclohex-1-enylmethyl)amine

https://huagongshe.com/reaction/131533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-[(Benzylmethylamino)methyl]-1-pyridin-3-ylcyclohexanol hydrochlorideHCID 69221643—
ProductBenzylmethyl-(2-pyridin-3-ylcyclohex-1-enylmethyl)amineHCID 6922035026.5%

Reaction Steps

5.5 g 2-[(benzylmethylamino)methyl]-1-pyridin-3-ylcyclohexanol hydrochloride and 27.5 ml thionyl chloride were heated at a bath temperature of 75° C. for one hour. After the mixture had been concentrated in vacuo, the residue was taken up in ethyl acetate and sodium hydroxide solution (32 percent strength by weight) and the organic phase was separated off, dried and concentrated. The crude product obtained (3.7 g) was chromatographed on silica gel with diisopropyl ether/ethyl acetate (V/V=2:1). 1.23 g benzylmethyl-(2-pyridin-3-ylcyclohex-1-enylmethyl)amine were obtained, and were dissolved in approx. 25 ml acetone and converted into the corresponding hydrochloride with 1.66 μl water and 1.18 ml chlorotrimethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384961B2
Source datasetuspto-grants-2008_06
ORD IDord-20e1fc51fa9244bca99efad335635a73
Source noteuspto-grants-2008_06