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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280165Generated: October 30, 2026

1,3-Dibromopropane → HCID 13799026, compound

https://huagongshe.com/reaction/280165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 131714666HCID 131714666—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDiethyl EtherHCID 3283—
ProductHCID 13799026HCID 13799026—

Reaction Steps

Potassium hydroxide (1.5 g, 10%) is added over a period of 1 hour 15 min to a stirred suspension of 3-hydroxy-1-(1-piperidinylmethyl)benzocyclobutene (1.0 g), and tetrabutylammonium chloride (0.13 g) in 1,3-dibromopropane (4.6 ml) and the resulting mixture stirred at RT under nitrogen for two days. The reaction mixture is partitioned between ice-water and ether and the aqueous layer separated and extracted with ether. The combined organic extract is washed with water, ice cold 5% aqueous HCl thereby forming a precipitate which is filtered and washed with ether. The acidic layer is alkalized forming an oily precipitate which is taken up in ether. The combined ether fractions are washed with water, dried over Na2SO4, filtered and concentrated in vacuo yielding the desired product as an oil which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588719
Source datasetuspto-grants-1986_05
ORD IDord-99959137c08b437cbbd1653b542580bd
Source noteuspto-grants-1986_05