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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248840Generated: October 27, 2026

Isopropanol → HCID 18651838, compound

https://huagongshe.com/reaction/248840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantIsopropylamineHCID 6363—
ReactantPotassium CarbonateHCID 11430—
ReactantN-[2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)ethyl]-N-(2-chloroethyl)-N-methylamine hydrochlorideHCID 67883408—
SolventWaterHCID 962—
ProductHCID 18651838HCID 18651838100%

Reaction Steps

5 g of N-[2-((1R,3R,4S)-1-methyl-4-isopropylcyclohex-3-yloxy)ethyl]-N-(2-chloro ethyl)-N-methylamine hydrochloride were added to a mixture of 50 ml isopropanol and 50 ml water. 1.9 g of isopropylamine and 7.7 g of potassium carbonate were then added, and the reaction mixture was heated under reflux for 5 hours. The reaction mixture was worked up by diluting it with 100 ml of water and extracting the solution with ethyl acetate. The organic phase was worked up as described in Example 1 C). 4.78 g of N-[2-((1R,3R,4S)-1-methyl-4-isopropylcyclo hex-3-yloxy)ethyl]-N-[2-(isopropylamino)ethyl]-N-methylamine were obtained. The free base was then converted into the corresponding hydrochloride analogously to Example 1 D). 5.1 g of N-[2-((1R,3R,4S)-1-methyl-4-isopropylcycl ohex-3-yloxy)ethyl]-N-[2-(isopropylamino)ethyl]-N-methylamine dihydrochloride having a melting point of 156° C.-158° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212173
Source datasetuspto-grants-1993_05
ORD IDord-10b6e182110646048ed7b9fb3d734569
Source noteuspto-grants-1993_05