HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl isothiocyanate → 4-Methyl-2-(methylamino)-1,3-benzothiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Amino-2-methylbenzoic acid | HCID 2733699 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methyl-2-(methylamino)-1,3-benzothiazole-5-carboxylic acid | HCID 18616049 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
99 g of 3-amino-2-methylbenzoic acid (0.655 mol) were initially charged in 500 ml of acetic acid and, at 80° C,. admixed with 51 g of methyl isothiocyanate (7 mol) in 100 ml of acetic acid. After 2 h, 106 g of bromine (0.66 mol) in 20 ml of acetic acid were added dropwise at 50° C. The mixture was subsequently heated at about 100° C. for 2 h and, after the reaction had ended, allowed to cool. The precipitate was filtered off, the filtrate was concentrated to about 50 ml and the remaining filtrate and the precipitate were added to water. The aqueous phase was adjusted to pH 5 and the precipitate was filtered off at 8° C. It was subsequently washed with water and dried. Yield: 66 g (42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541423B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-01832ae01f6b43ccbfa4faece788c228 |
| Source note | uspto-grants-2003_04 |