Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Acetylphenylacetonitrile | HCID 82505 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178419703 | HCID 178419703 | — |
Reaction Steps
To a stirred solution of 6.36 g. (0.04 mole) of p-acetylphenyl acetonitrile in 100 ml. of methylene chloride is added 6.40 g. (0.04 mole) of bromine in 50 ml. of methylene chloride. The reaction solution is warmed for a few minutes and the heat then removed. After a few minutes the bromine color disappears. The reaction mixture is stirred an additional 1/2 hour at room temperature. The methylene chloride is removed in vacuo on a rotary evaporator. To the residue is added 100 ml. of ethanol and 4.73 g. (0.04 mole) of amidinothiourea. The reaction mixture is heated with stirring for 1 hour under reflux, cooled in ice and then filtered. There is obtained 7.6 g. of product, m.p. 242°-246° (dec.). Recrystallization is from ethanol to which is then added enough water to form a solution. Ether is added to the cloudy point. There is obtained 5.9 g. of crystals, m.p. 259°-261° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04452985 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-42af59062f0b4aa9a09a4f18d914a98e |
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| Source note | uspto-grants-1984_06 |
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