HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 3-(Anilinomethyl)-1,3-benzothiazole-2(3H)-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 178418395 | HCID 178418395 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Anilinomethyl)-1,3-benzothiazole-2(3H)-thione | HCID 220471 | — |
Reaction Steps
With stirring, 18.63 (0.2 mole) of aniline are added to a suspension of 33.45 g (0.2 mole) of 2-mercaptobenzothiazole in 120 ml of ethanol, the temperature rising to 30° C. Then 16.4 g (0.2 mole) of 37% aqueous formaldehyde solution are added and stirring is continued for 30 minutes. The precipitate is isolated by filtration and washed with cold ethanol and hexane, affording 47 g of 3-(phenylaminomethyl)benzothiazoline-2-thione which melts at 102°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737302 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-a25db00b12044a95b69e1837bc8cddc5 |
| Source note | uspto-grants-1988_04 |