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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436428Generated: October 30, 2026

Bromomethylcyclopropane → 1,2,3,4,5,6-Hexahydro-3-cyclopropylmethyl-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocine

https://huagongshe.com/reaction/436428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethylcyclopropaneHCID 81503—
ReactantSodium BicarbonateHCID 516892—
Reactant1,2,3,4,-5,6-Hexahydro-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocineHCID 21325361—
SolventDimethylformamideHCID 6228—
Product1,2,3,4,5,6-Hexahydro-3-cyclopropylmethyl-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocineHCID 53787000—

Reaction Steps

A mixture of 1,2,3,4,5,6-hexahydro-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocine (part A, 0.220 g.), cyclopropylmethyl bromide (0.200 g.), sodium bicarbonate (0.084 g.) and N,N-dimethylformamide (5 ml.) was stirred in a nitrogen atmosphere under reflux (for 2 hr.), then stripped of N,N-dimethylformamide. A solution of the residue in dilute hydrochloric acid (5%) was extracted with ether, neutralized and extracted with ether again. Desiccation and concentration of the latter ether extracts afforded 1,2,3,4,5,6-hexahydro-3-cyclopropylmethyl-6-methyl-8-hydroxy-11-oxo-2,6-methano-3-benzazocine (I: Q = CH2CHCH2CH2, R = CH3, X = HO, Y + Z = O) as a yellow oil, from which with methanesulfonic acid was obtained the methanesulfonate salt as another oil, from which with 1,5-naphthalenedisulfonic acid was obtained the crystalline 1,5-naphthalenedisulfonate tetrahydrate salt (220 mg., m.p. 287°-288° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009171
Source datasetuspto-grants-1977_02
ORD IDord-d0062ddcaacb403cb3d024537cad8c86
Source noteuspto-grants-1977_02