HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266476Generated: October 27, 2026
tert-Butanol → 2-(4-methanesulfonylbenzyl)-3-oxobutyric Acid Ethyl Ester
https://huagongshe.com/reaction/2266476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 4-(Methylsulfonyl)benzyl Bromide | HCID 2733581 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-methanesulfonylbenzyl)-3-oxobutyric Acid Ethyl Ester | HCID 68780413 | — |
Reaction Steps
A suspension of potassium tert-butoxide (4.5 g) in anhydrous tetrahydrofuran (70 mL) at 0° C. was treated with a mixture of tert-butanol (0.2 mL) and 3-oxobutyric acid ethyl ester (5.2 g). After stirring at 15° C. for 15 minutes a solution of 1-bromomethyl-4-methanesulfonylbenzene (10 g) in tetrahydrofuran (30 mL) was added and the resulting mixture heated at 70° C. for 17 hours. The mixture was diluted with saturated aqueous citric acid solution (20 mL) and extracted with ethyl acetate. The combined extracts were washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of pentane and dichloromethane (2:1 to 0:1 by volume) to afford title compound as a gum, 3.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07858640B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-d355b4c00d4b4742af19560c8ee8cc27 |
|---|
| Source note | uspto-grants-2010_12 |
|---|