Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156654Generated: October 25, 2026

Dimethylformamide → 3,4-Bis(pivalyloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1156654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPivaloyl chlorideHCID 62493—
Reactant1-(3,4-Dihydroxyphenyl)-2-((1,1-dimethylethyl)amino)ethan-1-one hydrochlorideHCID 3015704—
ReactantPhenolate SodiumHCID 4445035—
ReactantSodium MethoxideHCID 10942334—
Product3,4-Bis(pivalyloxy)phenyl tert-butylaminomethyl ketoneHCID 12295036—

Reaction Steps

Proceeding in a manner similar to that described in part A of Example 2 above, 17 g. of sodium methoxide was interacted with 26 g. of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride in 200 ml. of N,N-dimethylformamide and the resulting sodium phenolate salt was interacted with 24 g. of pivalyl chloride (alternatively designated as trimethylacetyl chloride or 2,2-dimethylpropanoyl chloride). From this acylation reaction there was obtained 3,4-bis(pivalyloxy)phenyl tert-butylaminomethyl ketone which was treated with hydrochloric acid to yield 11.5 g. of 3,4-bis(pivalyloxy)phenyl tert-butylaminomethyl ketone hydrochloride as a white crystalline solid which melted at 243°-244° C. (dec.)(uncorr.). This salt was soluble in water at 25° C. to the extent of at least 1 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-775a9c81b882461abb5050aea140a667
Source noteuspto-grants-1982_06