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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874948Generated: November 1, 2026

Methanol → 5-(2-hydroxyethoxy)-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1874948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 86761647HCID 86761647—
SolventTetrahydrofuranHCID 8028—
Product5-(2-hydroxyethoxy)-1H-indole-2-carboxylic acidHCID 1845562216%
ProductHCID 68485440HCID 684854407%

Reaction Conditions

Temperature70 °C

Reaction Steps

A methanol solution of 1-(1,1-dimethylethyl)2-ethyl 5-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)oxy]-1H-indole-1,2-dicarboxylate (0.200 g, 0.431 mmol) was treated with 1 N LiOH (4 mL). A precipitate formed and THF was added to redissolve the material. The reaction was heated to 70° C. until the starting material was consumed, partitioned between EtOAc and water and the layers separated. The basic aqueous layer was acidified with conc. HCl and extracted with EtOAc. Purification was accomplished by silica gel column chromatography (0-100% EtOAc/hexanes, striped with MeOH) to afford the title compound (0.015 g, 16%) and 5-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)oxy]-1H-indole-2-carboxylic acid (0.0114 g, 7%) 1H NMR (400 MHz, Acetone-d6) δ ppm 10.73 (br. s., 1H), 7.43 (d, 1H), 7.15 (d, 1H), 7.10 (d, 1H), 6.96 (dd, 1H), 4.07 (t, 2H), 3.88 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-45ac2a52a60e41f3bce3c4b49340bdf9
Source noteuspto-grants-2012_11