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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474116Generated: October 29, 2026

Potassium tert-butoxide → HCID 86668086, compound

https://huagongshe.com/reaction/474116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86668084HCID 86668084—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
ProductHCID 86668086HCID 8666808671%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N—[(R)-1-(6-bromo-3-fluoro-4-triethylsilanyl-pyridin-2-yl)-2,2-difluoro-1-hydroxymethyl-ethyl]-2-chloro-acetamide (2.32 g, 4.88 mmol) in t-butanol (50 ml) was added potassium tert-butoxide (7.31 ml, 7.31 mmol, 1M in THF) and the solution was stirred in a closed vial for 18 h at 100° C. The reaction mixture was diluted with ethyl acetate, washed with water, sat. NaHSO4 solution and brine, dried over sodium sulfate, filtered and evaporated. The crude product (2.36 g) was chromatographed over silica gel (24 g redisep column, cyclohexane/ethyl acetate 10-80%) to give the title compound. 1.13 g (71% yield). Triethylsilylated lactam (640 mg) was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637508B2
Source datasetuspto-grants-2014_01
ORD IDord-e50b99160ca74b79bb3cab8be4f2823c
Source noteuspto-grants-2014_01