HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isothiocyanate → HCID 53716090, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14037275 | HCID 14037275 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53716090 | HCID 53716090 | — |
Reaction Steps
To a suspension of α-acetamido-p-aminophenylacetic acid (1.04 g, 5 mmol) in water (5 ml) was added 10% NaOH until solution was effected. The solution was diluted with an equal volume of ethanol and then t-butyl isothiocyanate (1.64 g, 15 mmol) in ethanol was added. The reaction was stirred at room temperature overnight and then refluxed 24 hours. The ethanol was evaporated in vacuo and the aqueous phase was acidified and filtered. The aqueous filtrate was extracted with ethyl acetate. The dried extracts were evaporated to give α-acetamido-p-(3-t-butylthioureido)phenylacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04091227 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-8ce5e191eb404c668782ab77d462b820 |
| Source note | uspto-grants-1978_05 |