Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Isopropylphenyl isothiocyanate | HCID 145194 | — |
| Reactant | 52031-05-7 | HCID 2723926 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10431373 | HCID 10431373 | 80% |
Reaction Steps
DL-4-Chlorophenylalanine ethyl ester hydrochloride(5 g, 18.9 mmol) was converted to the free base using triethylamine. A solution of the free base in 75 mL ether was added to a solution of 4-isopropylphenylisothiocyanate in 150 mL ether, cooled on an ice-salt bath. The temperature was maintained at about 0° C. during addition. The reaction was stirred for four and one-half hours, at which time the reaction temperature was 12° C.. The reaction mixture was filtered, the filtrate concentrated, and the resulting foamy residue triturated with petroleum ether while cooling on ice. This resulted in 6.1 g (15.1 mmol, 80%) N-(4-isopropylphenyl)-N'-[2-(4-chlorophenyl)-1-(ethoxycarbonyl)ethyl]thiourea, mp 73°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05296486 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-45e936e3dd4246ffb4aa3b90f03e3912 |
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| Source note | uspto-grants-1994_03 |
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