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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468216Generated: November 2, 2026

Acetone → HCID 12892725, compound

https://huagongshe.com/reaction/1468216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
Reactant2,2,4,4-Tetramethylcyclohexan-1-oneHCID 58388197—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 12892725HCID 1289272594%

Reaction Steps

To a stirred solution of 2 (1.98 mmol, 360 mg) in acetone (7.76 mL) was added 10% aqueous hydrochloric acid solution (3.02 mL), and the resulting mixture was stirred at room temperature for 2.5 hours. The reaction mixture was then diluted with brine (40 mL) and extracted with methylene chloride/ethyl ether (1:2, 3×30 mL). The organic layers were combined and washed with saturated aqueous sodium bicarbonate solution (2×30 mL) and brine (1×30 mL), then dried over magnesium sulfate, filtered, and concentrated in vacuo to give 19 (251.6 mg, 1.92 mmol, 94%) as a yellow oil that was used in the next reaction without further purification: 1H NMR (CDCl3) δ 5.89 (1H, dd, J=0.5, 17.3 Hz), 5.15 (1H, dd, J=1, 3.5 Hz), 5.12 (1H, dd, J=0.5, 10 Hz), 2.42-2.28 (4H, m), 1.97-1.91 (2H, m), 1.74-1.68 (2H, m), 1.12 (3H, s); 13C NMR (CDCl3) δ 212.4, 145.5, 112.9, 38.2, 37.1, 27.4; MS (EI) m/z 138.1 [M+], 123.1, 110.1, 105.1, 97.1, 86.0 (100%), 68.1, 63.0, 54.9; HRMS (EI) calcd for C9H14O 138.1045 found 138.1048.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000188B2
Source datasetuspto-grants-2015_04
ORD IDord-26430c305a444f9e821d0fa7ff3ed3ba
Source noteuspto-grants-2015_04