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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577837Generated: October 26, 2026

2,2,6,6-Tetramethylpiperidine → 2,4-Difluoro-5-[hydroxy(1,3-thiazol-2-yl)methyl]-3-methylbenzoic acid

https://huagongshe.com/reaction/577837

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1,3-Thiazole-2-carbaldehydeHCID 2734903—
Reactant2,4-Difluoro-3-methylbenzoic acidHCID 13986837—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,4-Difluoro-5-[hydroxy(1,3-thiazol-2-yl)methyl]-3-methylbenzoic acidHCID 86658058—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1.9 M n-BuLi (3.8 ml, 7.2 mmol) in hexanes was added at −30° C. to a stirred solution of 2,2,6,6-tetramethylpiperidine (1.2 g, 9.0 mmol) in THF and the mixture was stirred for an hour at the same temperature. After cooling to −78° C., a solution of 2,4-difluoro-3-methylbenzoic acid (Intermediate 46, 0.5 g, 3.0 mmol) in THF was added slowly at and the mixture was stirred for another 2 h at the same temperature. To this mixture, a solution of thiazole-2-carboxaldehyde (0.8 g, 7.2 mmol) in THF was added dropwise over a period of 10 mins and the mixture was brought to the room temperature. The reaction mixture was quenched with 1.5N hydrochloric acid and the organic layer was separated, the aqueous layer was extracted with ethyl acetate (3×10 mL) and the combined organic layer was dried over sodium sulfate. Removal of solvent afforded the title compound as colorless product. Yield: 0.42 g (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040528B2
Source datasetuspto-grants-2015_05
ORD IDord-e0d276c218324247b3dc8d437024d88c
Source noteuspto-grants-2015_05