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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032270Generated: October 31, 2026

Methanol → HCID 70374323, compound

https://huagongshe.com/reaction/1032270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron trifluorideHCID 6356—
ReactantHCID 70374081HCID 70374081—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70374323HCID 70374323—

Reaction Steps

A solution of 600 mg (2.5 mmol) of 2-methyl-3-oxo-5-chloro-1,3,4,8,9,9a-hexahydro-2H-indeno[1,7-cd]azepine, a compound of Formula 16 prepared, for example, as described in Preparation 16, dissolved in 25 ml of THF was combined with 8 ml of a 1M solution of BF3.THF in tetrahydrofuran. The reaction mixture was stored at ambient temperature for 16 hours. A few ml of methanol was added dropwise and the solvents were removed under vacuum. The residue was treated with 25 ml of 5% HCl and digested on a steam bath for 3 hours. After cooling to ambient temperature, the aqueous solution was washed once with ether, made alkaline with NaOH, and extracted with ether. The ether extract was concentrated to give 2-methyl-5-chloro-1,3,4,8,9,9a-hexahydro-2H-indeno[1,7-cd]azepine, a compound of Formula I, as the free base; (HBr salt, ethanol, mp 279°-281° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957914
Source datasetuspto-grants-1990_09
ORD IDord-deeb7472af194764b1c821e9107fb1d8
Source noteuspto-grants-1990_09