Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949992Generated: November 1, 2026

Acetic Acid → Tert-butyl[2-(4-formylphenoxy)-1,1-dimethylethyl]carbamate

https://huagongshe.com/reaction/1949992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyridineHCID 1049—
Reactanttert-Butyl [2-(4-cyanophenoxy)-1,1-dimethylethyl]carbamateHCID 57934408—
ReactantHCID 178418950HCID 178418950—
CatalystNickelHCID 935—
SolventWaterHCID 962—
ProductTert-butyl[2-(4-formylphenoxy)-1,1-dimethylethyl]carbamateHCID 57934200—

Reaction Steps

The title compound was synthesized by referring to J. Chem. Soc., 1962, 3961. To a solution of sodium hypophosphite monohydrate (1.5 g) in water (3 ml) were sequentially added tert-butyl[2-(4-cyanophenoxy)-1,1-dimethylethyl]carbamate (500 mg), pyridine (10 ml) and acetic acid (5 ml). While stirring at room temperature, Raney nickel (50% suspension in water) (2 ml) was added dropwise to the reaction mixture and the solution was stirred for 15 minutes at room temperature and for 1 hour at 40° C. After filtration through celite pad and several wash with tetrahydrofuran and methanol, the solvent was evaporated in vacuo, and the residue was neutralized by adding a saturated aqueous solution of sodium bicarbonate. After extraction with ethyl acetate, the solution was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (443 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-aeec60278c3f409781aa82aaed5d498c
Source noteuspto-grants-2013_03