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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | 4-(Tert-butoxy)-4-oxobutanoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051261B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b52d36544839492da0544b98ac9c6c1d |
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| Source note | uspto-grants-2015_06 |
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