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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951315Generated: November 4, 2026

Ammonia → HCID 11637442, compound

https://huagongshe.com/reaction/1951315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhosphoric AcidHCID 1004—
Reactant2-Methyl-1-[(4-methylphenyl)methyl]-1,2,3,4,5,6,7,8-octahydroisoquinolineHCID 13207807—
SolventWaterHCID 962—
ProductHCID 11637442HCID 1163744227.5%

Reaction Conditions

Temperature135 °C

Reaction Steps

(+)-1-p-methylbenzyl-2-methyl-1,2,3,4,5,6,7,8-octahydroisoquinoline (26.5 g) was added to 85% phosphoric acid (130 ml) and the mixture was heated to 130-140° C. for 72 h. After the reaction was complete, the reaction mixture was poured into ice-water and the solution was made strongly alkaline by the addition of conc. ammonia solution (about 300 ml) and diluted with water (500 ml). The solution was then extracted with ether (500 ml×2). The ether layers were combined and washed with water (200 ml), and dried (K2CO3), filtered and evaporated to yield an oil. The oil was immediately vacuum-distilled to produce a faint yellow oil (10 g; by 130-136° C./0.3 mm Hg) which was crystallized on standing. Recrystallization from acetone (˜10 ml) provided white prisms ((7.3 g) of (+)-3-methyl-17-methyl-morphinan; MS (ESI+): m/z 256 (M+1). This procedure is similar to the procedure in U.S. Pat. No. 3,786,054, incorporated by reference herein in its entirety.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404706B2
Source datasetuspto-grants-2013_03
ORD IDord-bc500054f19a49888824daddc8ede2e7
Source noteuspto-grants-2013_03