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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191651Generated: October 26, 2026

1-(3-Benzyloxybenzyl)-5-methoxy-2-phenylindole → 1-(3-Hydroxybenzyl)-5-methoxy-2-phenylindole

https://huagongshe.com/reaction/1191651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Benzyloxybenzyl)-5-methoxy-2-phenylindoleHCID 69671052—
SolventTrifluoroacetic acid water dimethylsulfideHCID 86597598—
Product1-(3-Hydroxybenzyl)-5-methoxy-2-phenylindoleHCID 6967091770%

Reaction Steps

1-(3-Benzyloxybenzyl)-5-methoxy-2-phenylindole (200 mg) was dissolved in trifluoroacetic acid-water-dimethyl sulfide (95/5/10, 4.8 mL), and the solution was stirred at room temperature for 68 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate. The solution was washed successively with a saturated aqueous sodium hydrogen carbonate solution and saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680120B2
Source datasetuspto-grants-2014_03
ORD IDord-017956df7c7b4e1596a409f3717b2702
Source noteuspto-grants-2014_03