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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653597Generated: October 29, 2026

Indole-3-Acetic Acid → Benzyl (1H-indol-3-yl)acetate

https://huagongshe.com/reaction/653597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-Acetic AcidHCID 802—
ReactantHCID 86744362HCID 86744362—
SolventHexaneHCID 8058—
ProductBenzyl (1H-indol-3-yl)acetateHCID 1960382780.4%

Reaction Steps

Indole 3-acetic acid 1 (9.45 g, 0.054 mol) was dissolved in methanolic benzyl diethyl anilinium hydroxide (0.54 mol) and the solvent removed in vacuo. The oily residue of the benzyl dimethyl anilinium salt was agitated with benzene, the benzene evaporated and the salt refluxed in toluene (170 ml, 1 h). Traces of unreacted acid and dimethyl aniline by-product were removed by extracting the toluene solution with water, dilute hydrochloric acid (1N) and water. The organic layer was dried over sodium sulphate and concentrated in vacuo to obtain the crude product. Final purification was obtained by crystallization in EtOAc:Hexane to give 11.52 g (80%) indole-3-acetic acid benzyl ester 13 as white crystals (melting point 71°-72° C.); IR (Nujol, cm-1); 3 400, 1, 720; 1H-NMR (CDCl3, δ): 3.8 (s, 2H), 5.1 (s, 2H) 6.8-8.0 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128164
Source datasetuspto-grants-1992_07
ORD IDord-4e8f61e9d5a049b48a4155ac93e2d1c8
Source noteuspto-grants-1992_07