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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349459Generated: October 29, 2026

[4-(5-{3-[3-(4-Fluorophenyl)prop-1-ynyl]phenyl}tetrazol-2-ylmethyl)phenoxy]acetic acid tert-butyl ester → [4-(5-{3-[3-(4-Fluorophenyl)prop-1-ynyl]phenyl}tetrazol-2-ylmethyl)phenoxy]acetic acid

https://huagongshe.com/reaction/349459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(5-{3-[3-(4-Fluorophenyl)prop-1-ynyl]phenyl}tetrazol-2-ylmethyl)phenoxy]acetic acid tert-butyl esterHCID 68980311—
SolventTrifluoroacetic acidHCID 6422—
Product[4-(5-{3-[3-(4-Fluorophenyl)prop-1-ynyl]phenyl}tetrazol-2-ylmethyl)phenoxy]acetic acidHCID 6897696062.3%

Reaction Steps

A solution of [4-(5-{3-[3-(4-fluorophenyl)prop-1-ynyl]phenyl}tetrazol-2-ylmethyl) phenoxy]-acetic acid tert-butyl ester (0.19 g. 0.38 mmol) in trifluoroacetic acid (“TFA”) (6 mL) was stirred at room temperature for 75 minutes, then evaporated to dryness. The residue was triturated with ether, evaporated, triturated again with ether/hexanes, evaporated, then triturated with hexanes/ethyl acetate 3:1. The solid was collected by filtration, washed with hexanes/ethyl acetate 3:1 and dried to give 0.1047 g of orange solid (59.11% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179822B2
Source datasetuspto-grants-2007_02
ORD IDord-67c5783a191b4f128e1ec39688a5a56f
Source noteuspto-grants-2007_02