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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527263Generated: November 2, 2026

5-Benzyloxyindole → HCID 68283428, compound

https://huagongshe.com/reaction/1527263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BenzyloxyindoleHCID 14624—
ReactantHCID 68284065HCID 68284065—
CatalystPalladiumHCID 23938—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 68283428HCID 68283428—

Reaction Steps

To a solution of (3-acetyl-5-benzyloxy-indol-1-yl)-acetic acid tert-butyl ester (MS: 380.0 [M+H]+; tR (HPLC conditions c): 5.72 min; prepared from 5-benzyloxy-1H-indole [1215-59-4] in a similar manner as described in Scheme A13 (step A and B)) (3.3 g, 8.70 mmol) in CH2Cl2/MeOH (80 mL) was added Pd/C (0.093 g, 0.870 mmol). The reaction mixture was stirred at RT for 5 h under H2 atmosphere. The reaction mixture was filtered over a pad of Celite and washed with CH2Cl2 and MeOH. Volatiles were evaporated, and the crude mixture was purified by flash chromatography on silica gel (gradient c-hexane/EtOAc 2:1 to 100% EtOAc). TLC, Rf (c-hexane/EtOAc 1:1)=0.35; MS: 312.0 [M+Na]+; tR (HPLC conditions c): 4.27 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-d815ddfc2c544864845d46550a40571d
Source noteuspto-grants-2015_07