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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376102Generated: October 31, 2026

Potassium tert-butoxide → HCID 69009594, compound

https://huagongshe.com/reaction/1376102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 85879299HCID 85879299—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69009594HCID 6900959486%

Reaction Steps

Under nitrogen, stir and cool to 0° C. a solution [(4-chloro-2-cyanophenyl)-(2,2,2-trifluoro-ethanoyl)amino]-acetic acid ethyl ester (93.34 g, 10 mmol) in tetrahydrofuran (20 mL) and add, dropwise, a 1M solution of potassium tert-butoxide in tetrahydrofuran (12 mL, 12 mmol). Stir the reaction at ambient temperature for 2 h and then partition between aqueous ammonium chloride/ethyl acetate. Separate the organic layer, dry over MgSO4, filter and concentrate to a solid. Triturate the solid with heptane, filter the solid and air dry to obtain 2.86 g (86%) of the title compound: MS 335(M+H), m.p. 249–251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169925B2
Source datasetuspto-grants-2007_01
ORD IDord-39c304eb5a504e639e12f27fe3927a7e
Source noteuspto-grants-2007_01