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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252038Generated: October 27, 2026

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

https://huagongshe.com/reaction/252038

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 numberUS07868002B2
Source datasetuspto-grants-2011_01
ORD IDord-f10f7196a4964cd995d2b27e131b8cda
Source noteuspto-grants-2011_01