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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6723Generated: October 26, 2026

tert-Butanol → (4-Phenyl-but-3-ynyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/6723

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-phenylpent-4-ynoic AcidHCID 10975983—
SolventTolueneHCID 1140—
Product(4-Phenyl-but-3-ynyl)-carbamic acid tert-butyl esterHCID 23544319—

Reaction Steps

A solution of 5-phenylpent-4-ynoic acid (0.49 g), diphenylphosphoryl azide (0.66 mL) and triethylamine (0.43 mL) was refluxed in 15 mL toluene for 3 h. The reaction was cooled to rt and t-butyl alcohol was added. The reaction was refluxed for 16 h, then the volatile materials were removed via a rotary evaporator. The residue was purified by column chromatography on silica (2–6% ethyl acetate in hexanes) to give (4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester (0.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084154B2
Source datasetuspto-grants-2006_08
ORD IDord-5939bb060647439fbc9218ef92c27765
Source noteuspto-grants-2006_08