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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420370Generated: October 31, 2026

Phenylboronic Acid → 4-{2-(2-Ethoxycarbonyl-ethyl)-3-[6-(5-thiophen-3-yl-biphenyl-3-yloxy)-hexyl]-phenoxy}-butyric acid ethyl ester

https://huagongshe.com/reaction/420370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant4-{3-[6-(3-Iodo-5-thiophen-3-yl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy}-butyric acid ethyl esterHCID 57586538—
Product4-{2-(2-Ethoxycarbonyl-ethyl)-3-[6-(5-thiophen-3-yl-biphenyl-3-yloxy)-hexyl]-phenoxy}-butyric acid ethyl esterHCID 5758644555.2%

Reaction Steps

A similar procedure as described in Example 12, step 8 was used, starting from 4-{3-[6-(3-iodo-5-thiophen-3-yl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy}-butyric acid ethyl ester (216 mg, 0.31 mmol) and phenylboronic acid (152 mg, 1.25 mmol) to give 4-{2-(2-ethoxycarbonyl-ethyl)-3-[6-(5-thiophen-3-yl-biphenyl-3-yloxy)-hexyl]-phenoxy}-butyric acid ethyl ester (110 mg, 55%) as a colorless oil: ES(+)-HRMS m/e calculated for C39H46O6S (M+Na)+ 665.2907, found 665.2907.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093385B2
Source datasetuspto-grants-2012_01
ORD IDord-10220a4b5d99444d8bf9e964359c033b
Source noteuspto-grants-2012_01