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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048040Generated: November 1, 2026

Tetrahydrofuran → tert-Butyl 4-(hydroxymethyl)phenethylcarbamate

https://huagongshe.com/reaction/1048040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(2-{[(Tert-butoxy)carbonyl]amino}ethyl)benzoic acidHCID 16640905—
Producttert-Butyl 4-(hydroxymethyl)phenethylcarbamateHCID 2233708085.2%

Reaction Steps

A 1M solution of borane-tetrahydrofuran complex in tetrahydrofuran (100 mL, 100 mmol) was added directly to solid (4-(2-(tert-butoxycarbonylamino)ethyl)benzoic acid (12.4 g, 46.7 mmol). The resulting solution was stirred at ambient temperature for 1 hour, carefully quenched with water (250 mL), and extracted with ethyl acetate (500 mL). The organic layer was washed with saturated sodium bicarbonate (200 mL) and brine (100 mL), dried over sodium sulfate and concentrated to afford tert-butyl 4-(hydroxymethyl)phenethylcarbamate as a pale yellow oil (10.0 g, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569522B2
Source datasetuspto-grants-2013_10
ORD IDord-41c6f7487c9c41febaae7abcefe6b0f2
Source noteuspto-grants-2013_10