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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651622Generated: November 1, 2026

Ethyl Acetate → HCID 54291701, compound

https://huagongshe.com/reaction/1651622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 53643109HCID 53643109—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54291701HCID 54291701—

Reaction Steps

10-Chloro-3-cyano-6,12-dimethyl-1,2,3,4,5,6-hexahydro-2,6-methano-9H-pyrrolo[3,2-h][3]benzazocine (6.41 g) was dissolved in 300 ml of tetrahydrofuran, and with stirring, 4.06 g of lithium aluminum hydride was added, under nitrogen. The suspension was heated at reflux for 2 hr and ethyl acetate was added dropwise. To the mixture was added water, 15% aqueous sodium hydroxide solution, and water. The suspension was filtered, and the filtrate was concentrated. The residue was triturated with ether. The mother liquor was concentrated and 2-g portions of the residue were alkylated with phenethyl bromide and 4-bromo-2-methylbut-2-ene according to the procedures described in Examples 23 and 26 to give 0.35 g (20%) and 0.41 g (24%), respectively, of product. Column chromatography (alumina, ether) followed by recrystallization from dichloromethane-ether-pentane afforded the analytical sample, mp 208°-210° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929622
Source datasetuspto-grants-1990_05
ORD IDord-d7bfbc26d53241fe98c2ef9e9b1e4db6
Source noteuspto-grants-1990_05