HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61307Generated: October 29, 2026
Jwh 250 → 2-(2-hydroxyphenyl)-1-(1-pentyl-1H-indol-3-yl)ethanone
https://huagongshe.com/reaction/61307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Jwh 250 | HCID 44397540 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-hydroxyphenyl)-1-(1-pentyl-1H-indol-3-yl)ethanone | HCID 86691090 | 29.2% |
Reaction Steps
2-(2-Methoxyphenyl)-1-(1-pentyl-1H-indol-3-yl)ethanone (JWH-250) 4 (3 g, 8.94 mmol) was dissolved in anhydrous dichloromethane (40 ml) and cooled at −78° C. A solution of 1NBBr3 (9.83 ml, 9.83 mmol) was added dropwise and once the addition was complete the reaction mixture was allowed to warm up to room temperature and was stirred at room temperature overnight. The reaction mixture was poured into a solution of 2NHCl (100 ml) and stirred for 30 min, then extracted three times with dichloromethane (3×150 ml) and the combined organic fractions dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (Biotage Isolera 4, SNAP-50 g, 0%-20% ethyl acetate in hexane) to give 840 mg (29%) of 2-(2-hydroxyphenyl)-1-(1-pentyl-1H-indol-3-yl)ethanone (O-desmethyl JWH-250) 5 as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09441033B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-344a8cb10cd14784be1c49bc42103ae5 |
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| Source note | uspto-grants-2016_09 |
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