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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621504Generated: November 2, 2026

Sodium Hydroxide → HCID 21243176, compound

https://huagongshe.com/reaction/621504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14074107HCID 14074107—
ReactantHCID 15576452HCID 15576452—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 21243176HCID 2124317691.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 3.605 g (10 mmol) of 1-(4-hydroxyphenyl)-4-(2-methyl-4-(4-tolyl)pyrimidin-6-yl)piperazine, 80 ml of toluene, 4.20 g (10 mmol) of 2-bromomethyl-2-(2,4 -dichlorophenyl)-4-methanesulfonyloxymethyl-1,3-dioxolane (cis/trans mixture), 0.65 g of tetrabutylammonium bromide and 13.5 ml of 50% strength sodium hydroxide solution was stirred vigorously for 4 hours at 55° C. The phases were subsequently separated at room temperature, the sodium hydroxide solution was extracted by shaking three times with ether, and the tolune and ther phases were combined. These were washed three times with water, dried, filtered and evaporated in vacuo. The residue remaining (7.4 g) was chromatographed on a silica gel S/CH2Cl2 column (diameter 2.6 cm, height 11 cm) with elution using CH2Cl2. After elution, the fractions which were unary according to TLC were combined and evaporated in vacuo. 6.27 g (=91.6% yield) of 2-bromomethyl-2 -(2,4-dichlorophenyl)-4-[4-(4-(2-methyl-4-(4-tolyl)pyrimidin-6-yl)piperazin-1-yl)phenoxymethyl]-1,3-dioxolane (cis/trans mixture) were obtained as a highly viscous oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824846
Source datasetuspto-grants-1989_04
ORD IDord-1dad5e0ea8a444f19f6c3be0c82d5721
Source noteuspto-grants-1989_04