HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester | HCID 69974681 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid | HCID 18180982 | — |
Reaction Steps
The 5-phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester from Step 64a (1.0 g, 3.76 mmol, 1 eq) is dissolved in EtOH (40 mL), and cooled in an ice bath. To this, 2N NaOH (1.88 mL 3.76 mmol, 1 eq) is added drop wise. The sodium salt of the acid precipitates out of solution. The reaction mixture is concentrated in vacuo to give a white crystalline product. The reaction mixture is carried through to the next step in its crude form to make the acid chloride. MS (ESI) for C9H6N2S2O2 m/z 237.0 (M−M)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492385B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-90c320f724c24fe5b82415c5126d7588 |
| Source note | uspto-grants-2002_12 |