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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61306Generated: October 26, 2026

Water → Jwh 250

https://huagongshe.com/reaction/61306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromopentaneHCID 8057—
ReactantSodium hydrideHCID 24758—
Reactant1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanoneHCID 43339287—
SolventDimethylformamideHCID 6228—
ProductJwh 250HCID 4439754049%

Reaction Steps

60% Sodium hydride in mineral oil (1.8 g, 45.23 mmol) was suspended in dimethylformamide (100 ml) and 1-(1H-indol-3-yl)-2-(2-methoxyphenyl)ethanone 3 (10 g, 37.70 mmol) was added portionwise at room temperature, allowing to stir further 45 min at room temperature after the addition was finished. 1-Bromopentane (7.02 ml, 56.55 mmol) was added dropwise at room temperature and the reaction mixture was stirred at room temperature overnight. Water (200 ml) was added and the mixture was extracted three times with ethyl acetate (3×200 ml). The organic fractions were combined, washed with water (200 ml) and brine (200 ml) and dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (Biotage Isolera 4, SNAP-100 g, 5%-20% ethyl acetate hexane containing 5% dichloromethane) to give 6.2 g (41%) of 2-(2-methoxyphenyl)-1-(1-pentyl-1H-indol-3-yl)ethanone (JWH-250) 4 as an orange/tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09441033B2
Source datasetuspto-grants-2016_09
ORD IDord-400ac1010ebe48afbdd94ee843771965
Source noteuspto-grants-2016_09