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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170261Generated: October 29, 2026

tert-Butanol → 4-(Tert-butoxy)-4-oxobutanoic acid

https://huagongshe.com/reaction/2170261

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSuccinic anhydrideHCID 7922—
ReactantN-HydroxysuccinimideHCID 80170—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Product4-(Tert-butoxy)-4-oxobutanoic acidHCID 4139107—

Reaction Steps

Sodium 2,2-d2-4-hydroxybutyrate is prepared in the following manner: treatment of succinic anhydride with tert-butanol, N-hydroxysuccinimide, and 4-dimethylaminopyridine (4-DMAP) according to the procedure of Yao, Z-J., et al, J. Org. Chem. 2003, 68, 6679-6684 affords the succinic acid mono-tert-butyl ester. In accordance with Yao, reduction of the succinic acid with borane-dimethyl sulfide complex gives the 4-hydroxybutanoic acid tert-butyl ester. Subjecting the ester to hydrogen/deuterium exchange by treatment with potassium carbonate in d1-methanol affords the 2,2-d2-4-hydroxybutanoic acid tert-butyl ester. Finally, saponification of the tert-butyl ester with sodium hydroxide in d1-methanol in a manner analogous to the procedure of Goto, G., et al, Chem. Pharm. Bull. 1985, 33, 4422-4431 affords the desired sodium 2,2-d2-4-hydroxybutyrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051261B2
Source datasetuspto-grants-2015_06
ORD IDord-b52d36544839492da0544b98ac9c6c1d
Source noteuspto-grants-2015_06