HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pentanamine → 2-(1-Methylbutyl)benzisothiazolin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pentanamine | HCID 12246 | — |
| Reactant | 2-(Chlorothio)-benzoyl chloride | HCID 10910715 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(1-Methylbutyl)benzisothiazolin-3-one | HCID 19595697 | — |
Reaction Steps
2-Chlorosulphenylbenzoyl chloride (6 parts, 0.029M) dissolved in diethylether (30 ml) was added dropwise at 0 to 3° C. to a stirred solution of 1-methylbutylamine (7.36 parts, 0.84M ex Aldrich) in diethylether (30 ml). The reactants were stirred for 16 hours whilst allowing the temperature to rise to about 20° C. The ether solution was then screened, washed with water and dried over magnesium sulphate. After evaporation of the ether, the product was obtained as a pale yellow gum (5.5 parts, 86% theory) which gradually solidified on standing. This was recrystallised from hexane. mp=52-54° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005032 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-3a564361bbf14d2e93e13e20369b47bf |
| Source note | uspto-grants-1999_12 |