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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082667Generated: November 1, 2026

Hydrochloric Acid → HCID 20360233, compound

https://huagongshe.com/reaction/2082667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl bromideHCID 7841—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20026446HCID 20026446—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 20360233HCID 20360233—

Reaction Steps

1.87 g of 2,3,4,5,6,7-hexahydro-1,6-methano-1H-4-benzazonine, 1.25 g of sodium bicarbonate and 1.33 g of allyl bromide were added into 30 ml of methanol, and the mixture was refluxed for 5 hours and subjected to distillation under reduced pressure. The residue was dissolved in 15 ml of 10% hydrochloric acid. The solution was washed once with 5 ml of benzene, and the water layer was made alkaline with sodium hydroxide and extracted with ether. Ether was distilled from the ether extract and the residue was subjected to vacuum distillation to obtain 2 g of a colorless oily substance as a fraction boiling at 110° to 120° C. (bath temperature) under 0.7 mmHg. The product was dissolved in 15 ml of ether and gaseous hydrochloric acid was blown into the solution to form a white precipitate. The precipitate was recovered by filtration and dried to obtain 4-allyl-2,3,4,5,6,7-hexahydro-1,6-methano-1H-4-benzazonine hydrochloride. Recrystallization from isopropanol gave a white crystalline powder melting at 212.5° to 214.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082744
Source datasetuspto-grants-1978_04
ORD IDord-039a74f4160c47b395992776cbab18c4
Source noteuspto-grants-1978_04