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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072361Generated: November 2, 2026

1,5-Dibromopentane → HCID 21407936, compound

https://huagongshe.com/reaction/2072361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl bromo(4-chlorophenoxy)acetateHCID 12376161—
ReactantHCID 21407938HCID 21407938—
ReactantHCID 57241026HCID 57241026—
Solvent1-ButanolHCID 263—
ProductHCID 21407936HCID 21407936—

Reaction Steps

2.3 g. of 1,5-dibromopentane, 3.2 g. of (4-chlorophenoxy)-(4-aminophenoxy)-acetic acid ethyl ester [obtainable by reacting Na-4-nitrophenolate with α-bromo-α-(4-chlorophenoxy)-acetic acid ethyl ester to obain the ethyl ester of (4-chlorophenoxy)-(4-nitrophenoxy)-acetic acid and subsequent hydrogenation], and 1.4 g. of K2CO3 are refluxed for 12 hours in 40 ml. of n-butanol. As an intermediate compound, the ethyl ester of (4-chlorophenoxy)-[4-(5-bromopentylamino)-phenoxy]-acetic acid is produced. After working up the mixture as usual, (4-chlorohenoxy)-(4-piperidinophenoxy)-acetic acid ethyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051170
Source datasetuspto-grants-1977_09
ORD IDord-60bee018ddd545439c9c7c075783bad3
Source noteuspto-grants-1977_09