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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361880Generated: October 30, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → tert-butyl N-methyl-N-(4-oxocyclohexyl)carbamate

https://huagongshe.com/reaction/2361880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant(3,3-Dimethyl-1,5-dioxa-spiro[5,5]undec-9-yl)-methyl-carbamic acid tert-butyl esterHCID 66891864—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Producttert-butyl N-methyl-N-(4-oxocyclohexyl)carbamateHCID 2482032889.1%

Reaction Steps

To a solution of (3,3-dimethyl-1,5-dioxa-spiro[5,5]undec-9-yl)-methyl-carbamic acid tert-butyl ester (1.27 g, 3.63 mmol, 1.0 eq.) in acetone (40 mL) and water (20 mL) was added PPTS (228 mg, 0.25 eq.) and the resulting reaction was heated to reflux overnight, cooled to room temperature, concentrated to 20 mL, poured in saturated NaHCO3 and extracted with 3×EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (hexanes to 20% EtOAc/hexanes) to give methyl-(4-oxo-cyclohexyl)-carbamic acid tert-butyl ester (735 mg, 88%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-57bbf066482e49208e5deae289551622
Source noteuspto-grants-2014_04