Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156677Generated: October 27, 2026

Phenolate Sodium → 3-(3,3-Dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1156677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolate SodiumHCID 4445035—
ReactantSodium MethoxideHCID 10942334—
ReactantNeoheptanoyl chlorideHCID 14921487—
Reactant3-Hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketoneHCID 54189973—
Product3-(3,3-Dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketoneHCID 54114160—

Reaction Steps

Following a procedure similar to that described in Example 2A above, when 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is interacted with 3,3-dimethylbutanecarbonyl chloride there is obtained 3-(3,3-dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone which reacts with hydrochloric acid to yield the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using the procedure described above in Example 2B, there is obtained 3-(3,3-dimethylbutanecarbonyloxy)-4-(p-toluyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-1e193545b1a2464cb2f2dec0bd88387a
Source noteuspto-grants-1982_06