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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083374Generated: October 26, 2026

Water → 5-(4-isopropylmorpholin-2-yl)methyl-10,11-dihydro-5H-dibenzo[a,d]cycloheptene

https://huagongshe.com/reaction/2083374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant10,11-dihydro-5H-dibenzo(a,d)cyclohepteneHCID 70029—
Reactant2-(Chloromethyl)-4-(propan-2-yl)morpholineHCID 12832480—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-(4-isopropylmorpholin-2-yl)methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 12832481—

Reaction Steps

A solution of n-butyl lithium in n-hexane (1.6 N, 1.6 ml) was added to 10,11-dihydro-5H-dibenzo[a,d]cycloheptene (390 mg) in anhydrous tetrahydrofuran at room temperature, and the resulting mixture was stirred under reflux for 40 minutes. A solution of 2-chloromethyl-4-isopropylmorpholine (362 mg) in benzene was added thereto while stirring under heating, and the resulting mixture was stirred under reflux for 4 hours, followed by addition of excess water. The reaction mixture was extracted with ethyl acetate. The ethyl acetate extract was dried, evaporated and chromatographed to afford 5-(4-isopropylmorpholin-2-yl)methyl-10,11-dihydro-5H-dibenzo[a,d]cycloheptene as oily material. M.P., 219° - 221° C (hydrochloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085210
Source datasetuspto-grants-1978_04
ORD IDord-f23ede89ffda4f6488634d59163d47a1
Source noteuspto-grants-1978_04