HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474116Generated: October 29, 2026
Potassium tert-butoxide → HCID 86668086, compound
https://huagongshe.com/reaction/474116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86668084 | HCID 86668084 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86668086 | HCID 86668086 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637508B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-e50b99160ca74b79bb3cab8be4f2823c |
|---|
| Source note | uspto-grants-2014_01 |
|---|