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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701632Generated: October 25, 2026

Phenolate Sodium → 3-(1,3-Dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1701632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolate SodiumHCID 4445035—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Hydroxy-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketoneHCID 12295018—
Reactant1,3-Dimethylcyclobutanecarbonyl chlorideHCID 20535379—
Product3-(1,3-Dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketoneHCID 20535395—

Reaction Steps

Following a procedure similar to that described in Example 13A above, when 3-hydroxy-4-(isovaleryloxy)phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is reacted with 1,3-dimethylcyclobutanecarbonyl chloride there is obtained 3-(1,3-dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)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 13B, there is obtained 3-(1,3-dimethylcyclobutanecarbonyloxy)-4-(isovaleryloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030241
Source datasetuspto-grants-1980_03
ORD IDord-04aaf9f3ded94811a4defc9d2c3677ff
Source noteuspto-grants-1980_03