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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242509Generated: November 3, 2026

3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine → {2-Methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl ester

https://huagongshe.com/reaction/1242509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridineHCID 21935751—
Reactant(4-Hydroxy-2-methyl-phenylsulfanyl)-acetic acid tert-butyl esterHCID 67072245—
Product{2-Methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl esterHCID 67072399—

Reaction Steps

In analogy to the procedure described in example 20A], (4-hydroxy-2-methyl-phenylsulfanyl)-acetic acid tert-butyl ester (example 20C]), was reacted with 3-chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine (example 1N]) to give {2-methyl-4-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethoxy]-phenylsulfanyl}-acetic acid tert-butyl ester, which was subsequently saponified in analogy to the procedure described in example 20B] to yield the title compound as white solid of mp. 168–169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-76d191a87f2b4ba6960fade82f3019c2
Source noteuspto-grants-2006_10