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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373487Generated: October 30, 2026

Ethyl 5-(phenylmethoxy)-1H-indole-2-carboxylate → [5-(Benzyloxy)-1H-indol-2-yl]methanol

https://huagongshe.com/reaction/2373487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-(phenylmethoxy)-1H-indole-2-carboxylateHCID 95721—
ReactantAluminium lithium hydrideHCID 21226445—
Product[5-(Benzyloxy)-1H-indol-2-yl]methanolHCID 10682298—

Reaction Steps

The title compound was prepared from ethyl 5-(benzyloxy)-1H-indole-2-carboxylate and lithium aluminum hydride according to the procedure described in step 3 of Example 1. The product was obtained as a white solid, mp: 106-107° C. Mass spectrum (ESI, [M+H]+) m/z 254. 1H NMR (400 MHz, DMSO-d6) δ 10.80 (s, 1H), 7.45 (d, 2H, J=7.33 Hz), 7.37 (t, 2H, J=7.49 Hz), 7.30 (d, 1H, J=7.18 Hz), 7.20 (d, 1H, J=8.71 Hz), 7.04 (s, 1H), 6.74 (dd, 1H, J=8.70 and 1.46 Hz), 6.16 (s, 1H), 5.16 (t, 1H, J=5.49 Hz), 5.01 (s, 2H), 4.55 ppm (d, 2H, J=5.50 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459478B2
Source datasetuspto-grants-2008_12
ORD IDord-59937003a1ef4f5cb86bd01b77ec06a9
Source noteuspto-grants-2008_12