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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883479Generated: October 30, 2026

Hydrochloric Acid → HCID 11469684, compound

https://huagongshe.com/reaction/1883479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N-DimethylanilineHCID 949—
Reactanttert-ButanolHCID 6386—
ReactantCyclohexylacetyl chlorideHCID 2757989—
SolventDichloromethaneHCID 6344—
ProductHCID 11469684HCID 1146968484%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a 5° C. solution of dimethylaniline (320 ml, 2.54 mol) in t-butyl alcohol (480 ml) was added dropwise a solution of cyclohexyl-acetyl chloride (250.9 g, 1.56 mol) in dichloromethane (320 ml) over 30 min. At the end of the addition, the addition funnel was rinsed with dichloromethane (80 ml). The reaction mixture was stirred 90 min at 5° C. and then allowed to warm to room temperature. After 15 hours at room temperature, the reaction solution was heated to reflux for 6 hours and then cooled to 5° C. The cold reaction mixture was acidified with 6 n hydrogen chloride (640 ml) and extracted with ethyl acetate. The organic layer was washed with 1 N hydrogen chloride (860 ml), water (2×860 ml), saturated aqueous sodium bicarbonate solution (2×860 ml), and brine (860 ml). The organic solution was dried (magnesium sulfate), filtered, and concentrated (room temperature/20 mm Hg). The remaining liquid was distilled to afford the desired product as a yellow oil (259.32 g, 84%). bp.: 70-75° C./0.6 mm Hg; MS m/z: 199 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759420B1
Source datasetuspto-grants-2004_07
ORD IDord-417332d5a4b842a2834667a0b700c34d
Source noteuspto-grants-2004_07