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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919336Generated: November 2, 2026

Isobutyric Acid → Methyl 1-{[(alpha-Isobutanoyloxyisobutoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetate

https://huagongshe.com/reaction/1919336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyric AcidHCID 6590—
ReactantMethyl 1-{[(alpha-Chloroisobutoxy)carbonyl]aminomethyl}-1-Cyclohexane AcetateHCID 66584224—
CatalystHCID 178418647HCID 178418647—
SolventChloroformHCID 6212—
ProductMethyl 1-{[(alpha-Isobutanoyloxyisobutoxy)carbonyl]aminomethyl}-1-Cyclohexane AcetateHCID 6658435063.3%

Reaction Steps

A mixture of (106) (760 mg, 2.38 mmol), silver carbonate (394 mg, 1.4 mmol), and isobutyric acid (442 μL, 4.76 mmol) in chloroform was stirred at room temperature for 24 h. Another batch of silver carbonate (394 mg, 1.4 mmol) and isobutyric acid (442 μL, 4.76 mmol) was added, and the resulting mixture was stirred for another 24 h. After filtration, the filtrate was concentrated and the resulting residue purified by silica gel flash column chromatography, eluting with 10% ethyl acetate/hexane, to afford 560 mg (63%) of the title compound. 1H NMR (CDCl3, 400 MHz): δ 0.94 (d, J=6.8 Hz, 3H), 0.96 (d, J=6.8 Hz, 3H), 1.15 (d, J=7.2 Hz, 3H), 1.17 (d, J=7.2 Hz, 3H), 1.32-1.58 (m, 10H), 2.01 (m, 1H), 2.19 (s, 2H), 2.55 (m, 1H), 3.18 (m, 2H), 3.67 (s, 3H), 5.33 (t, 1H), 6.56 (d, J=4.8 Hz, 1H). MS (ESI) m/z 372.38 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168623B2
Source datasetuspto-grants-2012_05
ORD IDord-8ea0435e24f64b3893192ca05673905e
Source noteuspto-grants-2012_05