Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 2-Chlorothiazole | HCID 76429 | — |
| Reactant | 4-Chlorobenzyl cyanide | HCID 241582 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20361795 | HCID 20361795 | — |
Reaction Steps
At 0°-5° C add a suspension of 28.5 g. of sodamide in 300 ml. of toluene to a stirred solution containing 50 g. of p-chlorphenylacetonitrile and 40 g. of 2-chlorothiazole in 400 ml. of toluene. Maintain the temperature at 20° C for 2 hrs. and finally at 60° C for 1 hr. Consecutively add 100 ml. of water and 35 ml. of acetic acid at 0°-10° C and filter the resulting mixture. Separate the toluene layer, concentrate in vacuo and distill the residue to give α-(p-chlorphenyl)-2-thiazolylacetonitrile as a mobile yellow oil, b.p. 155°-160° C/1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04081544 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-7b9d68ca7a5142b79d5fa93c2787b0ce |
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| Source note | uspto-grants-1978_03 |
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