HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Benzyl-3-(tert-butylsulfonyl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | ethyl (RS)-alpha-[(tert-butylsulfonyl)methyl]hydrocinnamate | HCID 14158057 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzyl-3-(tert-butylsulfonyl)propanoic acid | HCID 14158058 | — |
Reaction Steps
550 mg of 2-benzyl-3-tert.-butylsulphonyl-propionic acid ethyl ester are dissolved in 8 ml of THF and then reacted with 5 ml of water and 0.88 ml of 2N potassium hydroxide solution. The mixture is stirred overnight at room temperature, neutralised with 0.88 ml of 2N hydrochloric acid and concentrated by evaporation. The residue is purified by flash chromatography on 30 g of silica gel 60 (eluant H). Yellow oil; m/e 284; 1H-NMR (DMSO-d6): 1.27 ppm (s, 9H); 2.73-3.1 (m, 4H); 3.2-3.5 (m, 1H); 7.2-7.4 (m, 5H); 12.5 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889869 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-24ce2ba82e984f12926ae1ea2361f496 |
| Source note | uspto-grants-1989_12 |