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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079236Generated: October 31, 2026

Benzoyl chloride, 3-nitro- → HCID 54295182, compound

https://huagongshe.com/reaction/1079236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantHCID 54185865HCID 54185865—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54295182HCID 54295182—

Reaction Steps

A 620 mg portion of (4aR)-(10bR)-4,10b-dimethyl-8-amino-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one was dissolved in 100 ml of THF, and an equivalent amount of 3-nitrobenzoyl chloride (500 mg) was added. The reaction mixture was stirred for 4 h, and was then evaporated to dryness under vacuum. The residue was purified by chromatography on silica gel, eluting with 10% methanol in ethyl acetate, and the product-containing fractions were evaporated and the resulting solid was crystallized from dichloromethane/hexane to obtain 595 mg of the desired product, m.p. 240°-242°. FDMS: m/e=393. α[D]589 =+75.79°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-1f9d83ed0131483882382c440de7d5fc
Source noteuspto-grants-1996_08