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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265124Generated: October 30, 2026

Chloromethyl pivalate → Pivaloyloxymethyl 2-ethyl-4-(1-hydroxy-1-methylethyl)-1-{4-[2-(trityltetrazole-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate

https://huagongshe.com/reaction/265124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl pivalateHCID 87885—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 2-ethyl-4-(1-hydroxy-1-methylethyl)-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylateHCID 19036058—
ProductPivaloyloxymethyl 2-ethyl-4-(1-hydroxy-1-methylethyl)-1-{4-[2-(trityltetrazole-5-yl)phenyl]phenyl}methylimidazole-5-carboxylateHCID 19036080100.2%

Reaction Steps

Following a procedure similar to that described in Example 78(a), but using 2.25 g of ethyl 2-ethyl-4-(1-hydroxy-1-methylethyl)-1-{4-[2-(trityltetrazole-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate [prepared as described in Example 68 (a)] and using 203 mg of lithium hydroxide monohydrate for hydrolysis and 0.90 g of pivaloyloxymethylchloride for esterification. 2.53 g of the title compound were obtained as a glass (purified by column chromatography through silica gel, using a 1:1 by volume mixture of ethyl acetate and hexane as the eluent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646171
Source datasetuspto-grants-1997_07
ORD IDord-41ac3e1af0d240a29cda22300a7c1640
Source noteuspto-grants-1997_07