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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763659Generated: November 1, 2026

Ethanol → HCID 54330103, compound

https://huagongshe.com/reaction/1763659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl orthoformateHCID 31214—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54400122HCID 54400122—
SolventEthyl AcetateHCID 8857—
ProductHCID 54330103HCID 54330103—

Reaction Steps

A solution of 9-amino-11-(3-dimethylaminopropylidene)-6,11-dihydro-5H-pyrrolo[2,1-b][3]benzazepine in triethyl orthoformate (2.8 g.; 10 mmoles in 80 ml.) was refluxed for 5 hours. The volatiles were removed under vacuum and the residue dissolved in 100 ml. of absolute ethanol was stirred in an ice bath as sodium borohydride (0.88 g., 0.024 moles) was added over a period of 10 minutes. The mixture was stirred for a period of 2 hours. After concentration of the ethanol, the residue was dissolved in ethyl acetate, washed with water, dried over Na2SO4 and concentrated to dryness to yield 9-methylamino-11-(3-dimethylaminopropylidene)-6,11-dihydro-5H-pyrrolo[2,1-b][3]benzazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112112
Source datasetuspto-grants-1978_09
ORD IDord-576f886ce1c74257927d852ad918d518
Source noteuspto-grants-1978_09