Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399983Generated: November 1, 2026

tert-Butanol → Docos-21-ynoic Acid. Tert.-Butyl Ester

https://huagongshe.com/reaction/2399983

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDocos-21-ynoic AcidHCID 54502951—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductDocos-21-ynoic Acid. Tert.-Butyl EsterHCID 8674900086.5%

Reaction Steps

The acid (32) (6.4 g, 0.019 mol) was dissolved in dry, ethanol free, chloroform (120 ml) at room temperature under nitrogen and sequentially treated with dimethylaminopyridine (2.55 g, 0.0209 mol), tert butanol (14.09 g, 0.19 mol), dimethylaminopyridine-trifluoroacetic acid complex (4.94 g, 0.0209 mol) and dicyclohexylcarbodiimide (4.31 g, 0.0209 mol). The resulting solution was stirred at room temperature overnight then filtered, the organic layer washed with 5% acetic acid in water, then dried (MgSO4), filtered and evaporated. The residue was purified by chromatography on silica gel (50 g). Elution with 10% ether in petrol gave the title compound (33) as white crystals (6.45 g, 86%) mp 44°-45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451691
Source datasetuspto-grants-1995_09
ORD IDord-855eab96cae946449702111060dc039e
Source noteuspto-grants-1995_09