HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 57151048, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | (2R)-2-Bromopropanoic acid | HCID 6992152 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57151048 | HCID 57151048 | 92% |
Reaction Steps
To a solution of 483 mg of Na in 10 mL of EtOH was added 10 mL of tert-butylthiol with stirring at room temperature under nitrogen. After 10 min a solution of 1.53 g of (2R)-2-bromopropanoic acid in 3 mL of EtOH was added and the stirring was continued at room temperature for 3 h. The reaction mixture was poured into water and was acidified with acetic acid and extracted with CH2Cl2. The organic layer was dried over Na2SO4 and was evaporated under water aspirator vacuum using a trap containing bleach to give 1.48 g of (2S)-2-(tert-butylthio)propanoic acid as an oil at 92% yield. Characteristic analytical data are as follows: 1H NMR (300 MHz, CDCl3) δ3.44 (q, J=7 Hz, 1H), 1.49 (d, J=7 Hz, 3H), 1.37 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05455262 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-c6d14cbecff049508155c47bb5dd0e02 |
| Source note | uspto-grants-1995_10 |