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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616608Generated: October 29, 2026

Ethanol → HCID 12909379, compound

https://huagongshe.com/reaction/616608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 13152853HCID 13152853—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTriethylamineHCID 8471—
ProductHCID 12909379HCID 12909379—

Reaction Steps

A suspension of 25 g. (0.070 mole) of 2,3-dibromo-6,11-dihydro-5 H-pyrrolo[2,1-b][3]benzazepin-11-one in 200 ml. ethanol containing 25 ml. of triethylamine and 1 gm. of 10% Pd on charcoal was hydrogenated under 3 atmospheres of hydrogen to yield 6,11-dihydro-5H-pyrrolo-[2,1-b][3]benzazepin-11-one, m.p. 54°-55° C. after removal of catalyst, recrystallization from petroleum ether and drying under vacuum. The same compound is also obtained by hydrogenolysis of the 2,3-dichloro ketone and the 1,2,3-tribromoketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075225
Source datasetuspto-grants-1978_02
ORD IDord-851ee8d9ae394760a9c3801f0269f95c
Source noteuspto-grants-1978_02