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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743220Generated: October 31, 2026

Dimethylamine → 1-{2-[4-(2-Chlorophenyl)butyl]phenoxy}-3-dimethylamino-2-propanol

https://huagongshe.com/reaction/743220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant2-{2-[4-(2-Chlorophenyl)butyl]phenoxymethyl}oxiraneHCID 19423926—
SolventTetrahydrofuranHCID 8028—
Product1-{2-[4-(2-Chlorophenyl)butyl]phenoxy}-3-dimethylamino-2-propanolHCID 1942391880%

Reaction Steps

Following a procedure similar to that described in Example 1(b), 860 mg of 2-{2-[4-(2-chlorophenyl)butyl]phenoxymethyl}oxirane [prepared as described in step (a) above] dissolved in 20 ml of tetrahydrofuran were treated with 4 ml of 50% by volume aqueous dimethylamine. The crude product thus obtained was purified as described in Example 1(b), to give 790 mg (yield 80%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556864
Source datasetuspto-grants-1996_09
ORD IDord-493f0a573e49440c9f9db719435b652c
Source noteuspto-grants-1996_09