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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920585Generated: October 31, 2026

tert-Butanol → Tert-butyl 3-bromobutanoate

https://huagongshe.com/reaction/920585

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-Bromobutanoic acidHCID 102860—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-bromobutanoateHCID 57092335—

Reaction Steps

3-{2-[4-(2,6-Dichloro-benzyloxy)-phenyl]-morpholin-4-yl}-butyric acid tert-butyl ester was obtained according to a similar manner. The required 3-bromobutyric acid tert-butyl ester was prepared as follows: To a solution of 3-bromobutyric acid (5.0 mL; 47.0 mmol) in tetrahydrofuran (50 mL) was added dropwise trifluoroacetic anhydride (13.7 mL; 98.7 mmol) at −40° C. After 1 hour at −40° C. tert-butyl alcohol (20 mL) was added. The resulting mixture was allowed to warm to RT and stirred overnight. Subsequently, the reaction mixture was concentrated in vacuo. The residue was treated with 2M aqueous NaOH solution and extracted with Et2O. The organic layer was dried (Na2SO4), and concentrated in vacuo to afford 3-bromobutyric acid tert-butyl ester (6.05 g), which was used as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-9f2230efa9b24e22b08182df5ca76526
Source noteuspto-grants-2016_03