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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708402Generated: October 29, 2026

Sulfuric Acid → (S)-tert-Butyl 2-chloropropanoate

https://huagongshe.com/reaction/708402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactanttert-ButanolHCID 6386—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant(S)-(-)-2-Chloropropionic acidHCID 107915—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyl 2-chloropropanoateHCID 11084226103.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Prepared according to Wright et al. Tetrahedron Lett. 1997, 38, 7345. A 500 mL glass bomb was charged with magnesium sulfate (21.7 g, 181 mmol) and DCM (182 mL). To this suspension was added sulfuric acid (2.5 mL, 45 mmol), drop-wise with vigorous stirring. After 15 min of stirring, (S)-2-chloropropanoic acid (5.0 g, 45 mmol) was added followed by tert-butanol (21.6 ml, 226 mmol). The bomb was sealed and stirred at rt for 19 h, whereupon it was cooled to 0° C. and sodium bicarbonate (aq satd, 350 mL) was carefully added, at which point all solids had dissolved. The layers were separated and the aqueous layer was extracted with DCM (2×). The combined organics layers were washed with brine, dried over Na2SO4 and concentrated in vacuo (20° C. bath, 50 mBar) to afford the title compound (7.64 g, 96%) as a light yellow oil (93% purity). 1H NMR data was an identical match to the previously prepared enantiomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-87e3fe566c49496bbd065ada9d49db33
Source noteuspto-grants-2015_11