Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476095Generated: October 25, 2026

Butanoyl chloride, 2-methyl- → Tert-butyl 2-methylbutanoate

https://huagongshe.com/reaction/1476095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoyl chloride, 2-methyl-HCID 93697—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-methylbutanoateHCID 52348332.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

15.0 g (124.4 mmol) of 2-methylbutyryl chloride were dissolved in 150 ml of abs. THF and cooled to 0° C., and 114 ml (114 mmol) of a 1 M solution of potassium tert-butylate in THF were added dropwise. After the addition had ended, the mixture was stirred at 0° C. for 1 h and then at RT for h, and about half of the solvent was then removed under reduced pressure. After addition of diethyl ether, sat. sodium bicarbonate solution was added dropwise with vigorous stirring. After phase separation, the aqueous phase was extracted with diethyl ether, and the combined organic phases were washed with sat. sodium carbonate solution, dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by vacuum distillation (19 mm Hg, 40-45° C.). This gave a total of 6.35 g of the target product (32.3% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018414B2
Source datasetuspto-grants-2015_04
ORD IDord-c2b13b313e564c8fb82b927cd1a695ee
Source noteuspto-grants-2015_04