HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 13131616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 13131604 | HCID 13131604 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 13131616 | HCID 13131616 | 58.7% |
Reaction Steps
4.4 g (0.031M) of benzoyl chloride in 10 ml of dimethoxyethane is dripped into a suspension of 2.5 g (0.033M) of ammonium thiocyanate in 50 ml of 1,2-dimethoxyethane. The mixture is stirred at room temperature for 1 hour. 4.5 g (0.028M) of 2-amino-4,7-dimethylisoindoline in 30 ml of dimethoxyethane are dripped in. The mixture is stirred at room temperature for 1 hour. The precipitated ammonium chloride is suctioned off. Evaporation yields 5.3 g of 1-benzoyl-3-(4,7-dimethylisoindolin-2-yl)-thiourea (Mp. 163°-164° C.) from the filtrate, which is converted by saponification with 50 ml of 10% sodium hydroxide into the (4,7-dimethylisoindolin-2-yl)-thiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04526897 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-2c6b5d933bdc43cb9412a3bc945ab7d4 |
| Source note | uspto-grants-1985_07 |