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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654939Generated: October 30, 2026

Benzyl Alcohol → 2-(Benzyloxycarbonylaminomethyl)indan

https://huagongshe.com/reaction/1654939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(2,3-dihydro-1H-inden-2-yl)acetic AcidHCID 5174955—
SolventTolueneHCID 1140—
Product2-(Benzyloxycarbonylaminomethyl)indanHCID 1892148386.4%

Reaction Steps

17.6 g (0.10 mol) of (indan-2-yl)acetic acid was dissolved in 150 ml of toluene, to which were added 15.3 ml (0.11 mol) of triethylamine and 33.0 g (0.12 mol) of diphenylphosphorylazide, and stirred at room temperature for 30 minutes. The mixture was added with 16.6 g (0.15 mol) of benzyl alcohol and refluxed for 18 hours. After cooling, the solvent was distilled under reduced pressure, and the residue was added with 500 ml of ethyl acetate, washed with 1N sodium hydroxide, and condensed. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:3), and the crystals collected were recrystallized from a solvent mixture of ethyl acetate and hexane to obtain 24.3 g of 2-(benzyloxycarbonylaminomethyl)indan as colorless needles. Yield: 86%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409956
Source datasetuspto-grants-1995_04
ORD IDord-cdd8da38ea0e4a7daae1763de9468670
Source noteuspto-grants-1995_04