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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607700Generated: October 30, 2026

Benzhydrol → HCID 19850789, compound

https://huagongshe.com/reaction/1607700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrolHCID 7037—
ReactantHCID 19850790HCID 19850790—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 19850789HCID 19850789—

Reaction Steps

10.1 g of benzhydrol are refluxed with 6.2 g of potassium tertiary butoxide in 100 ml of anhydrous tertiary butanol under argon gas for 30 minutes, then 19.6 g of 1-[3-[(4-fluorophenyl)-phenylmethoxy]propyl]-4-(2-chloroethyl)piperazine dissolved in 40 ml of anhydrous tertiary butanol are dropwise added. The mixture is boiled for one additional hour, then evaporated to about 40 ml under reduced pressure and after adding water it is extracted with benzene. The organic phase is dried over anhydrous magnesium sulfate and, after evaporating benzene under reduced pressure, the residue is fractionally distilled. The aimed compound boils at 247°-250° C./0.01 Hgmm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866062
Source datasetuspto-grants-1989_09
ORD IDord-b51c3398b23e4eb7b67e014885afa270
Source noteuspto-grants-1989_09