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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399480Generated: October 31, 2026

Hydrogen Bromide → JWH 018 5-hydroxyindole metabolite

https://huagongshe.com/reaction/1399480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant5-methoxy-3-(1-naphthoyl)-N-pentyl-1H-indoleHCID 68159293—
SolventWaterHCID 962—
ProductJWH 018 5-hydroxyindole metaboliteHCID 5339444772%

Reaction Steps

To a solution of hydrobromic acid (48 w/w %) in water (150 ml) was added 5 (6.5 g, 17.5 mmol) and the mixture was heated at reflux for 3 h. The solution was cooled to room temperature and concentrated to dryness. Water was then added (200 ml), the solution neutralized to pH 7-8 and then extracted with ethyl acetate (3×150 ml). The combined organic layers were washed by water (150 ml), brine (150 ml), dried over Na2SO4, filtered and concentrated to dryness. The crude product was then recrystallized from ethyl acetate/hexane to give a white solid of 5-hydroxy-3-(1-naphthoyl)-N-pentyl-1H-indole 6 (4.5 g, 72%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906633B2
Source datasetuspto-grants-2014_12
ORD IDord-844bb37dfeb04981ac4fa39fb140efd2
Source noteuspto-grants-2014_12