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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120086Generated: November 1, 2026

Triethylamine → Cyclohexanecarbaldehyde oxime

https://huagongshe.com/reaction/2120086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventDichloromethaneHCID 6344—
ProductCyclohexanecarbaldehyde oximeHCID 638165—

Reaction Steps

To a solution of cyclohexanecarbaldehyde (4 ml, 33.02 mmol) in CH2Cl2 (100 ml) at room temperature was added hydroxylamine hydrochloride (2.76 g, 39.62 mmol) followed by Et3N (5.52 ml, 39.62 mmol) and the reaction was stirred overnight. The resulting mixture was partitioned between CH2Cl2 and H2O and the layers were separated. The organic layer was dried over Na2SO4, concentrated in vacuo and used directly for the next step. 1H NMR (CDCl3) δ 1.0-2.0 (m, 10H), 3.0 (m, 1H), 6.6 (d, 0.5H), 7.4 (d, 0.5H), 8.2 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689778B2
Source datasetuspto-grants-2004_02
ORD IDord-1bf212870d684af7b5e5fcc427eeb240
Source noteuspto-grants-2004_02