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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247975Generated: October 25, 2026

4-(2-Morpholinoethoxy)benzaldehyde → 4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholine

https://huagongshe.com/reaction/2247975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Morpholinoethoxy)benzaldehydeHCID 3719902—
Reactant[1-(2,2-Dimethyl-1,3-benzodithiol-5-yl)ethyl]triphenylphosphonium bromideHCID 19935456—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholineHCID 8674496235.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

6.6 g of [1-(2,2-dimethyl-1,3-benzodithiol-5-yl)ethyl]triphenylphosphonium bromide were dissolved in 40 ml of tetrahydrofuran and treated slowly at 0° C. with 9 ml of a 1.5 molar solution of n-butyllithium in hexane. After 40 minutes, 3.5 g of 4-(2-morpholinoethoxy)benzaldehyde in 10 ml of tetrahydrofuran were added dropwise to the dark red solution and the mixture was stirred at 20° C. for 16 hours. The mixture was then poured on to ice and extracted with ethyl acetate. The combined extracts were washed with water, dried and evaporated. After chromatography (silica gel, eluting agent ethyl acetate) and crystallization from ether/hexane, there were obtained 1.8 g of 4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholine in the form of colorless crystals, melting point 90°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037825
Source datasetuspto-grants-1991_08
ORD IDord-19d8568ca4f84a77ad1434fd2f738c06
Source noteuspto-grants-1991_08