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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723028Generated: November 1, 2026

Sodium Hydroxide → HCID 20026482, compound

https://huagongshe.com/reaction/1723028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14074292HCID 14074292—
ReactantHCID 15576452HCID 15576452—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 20026482HCID 2002648272.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 3.77 g (14 mmol) of 4-(4-hydroxyphenyl)-1(pyrid-2-ylmethyl)piperazine, 200 ml of toluene, 5.88 g (14 mmol) of 2-bromomethyl-2-(2,4-dichlorophenyl)-4-methanesulfonyloxymethyl-1,3-dioxolane, 0.80 g of tetrabutylammonium bromide and 27 ml of 50% strength sodium hydroxide solution was stirred vigorously for 3 hours at 65° C. The phases were subsequently separated at room temperature. The toluene solution was shaken three times with water, dried, filtered and evaporated in vacuo. The residue remaining (8.8 g) was chromatographed on a silica gel S/CH2Cl2 column (diameter 2.6 cm, height 28.0 cm) with elution using CH2Cl2 and CH2Cl2 /C2 5OH mixtures (to a maximum C2H5OH content of 4% by volume). After elution of a preliminary fraction (1.45 g), the fractions which were unary according to TLC were combined and evaporated in vacuo. 6.02 g (=72.4% yield) of 2-bromomethyl-2-(2,4-dichlorophenyl)-4-[4-(4-(pyrid-2-ylmethyl)piperazin-1-yl)phenoxymethyl]-1,3-dioxolane (cis/trans mixture) were obtained as a highly viscous oil, analysis: C27H28BrCl2N3O3 (MW 593.38) calc. C 54.65, H 4.76, Br 13.47, Cl 11.95, N 7.08; found C 53.5, H 4.9, Br 13.1, Cl 13.2, N 6.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859670
Source datasetuspto-grants-1989_08
ORD IDord-070d35859b0e4731a955920922627b45
Source noteuspto-grants-1989_08