HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750565Generated: October 31, 2026
Phenoxycarbonyl isothiocyanate → HCID 178511143, compound
https://huagongshe.com/reaction/750565
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenoxycarbonyl isothiocyanate | HCID 12212046 | — |
| Reactant | 2-Cyano-acetimidic acid benzyl ester | HCID 29939191 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178511143 | HCID 178511143 | 42.4% |
Reaction Steps
To a stirred 0° C. solution of 2-cyano-acetimidic acid benzyl ester (327 g, 1.88 mol) in acetonitrile (1 L) was added a 0° C. solution of phenoxycarbonylisothiocyanate (353 g, 1.97 mol) in acetonitrile (1 L). The reaction was allowed to warm to ambient temperature and was stirred overnight. The mixture was then placed in the refrigerator and kept still at 5° C. for 48 hours. The solid product was filtered, compressed, and washed with 20° C. acetonitrile (3×200 mL). Air was then drawn though the relatively stable solid followed by further drying under high vacuum to yield a yellow solid (282 g, 798 mmol, 42%). 1H NMR (400 MHz, DMSO) δ 5.39 (s, 2H), 7.11-7.19 (m, 2H), 7.20-7.24 (m, 1H), 7.36-7.46 (m, 7H), 10.23 (broad s, 1H), 10.67 (s, 1H), 12.19 (broad s, 1H) ppm; MS (APCl, m/z): 354 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405218B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-cdce71499eab4966b5601542a030ce97 |
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| Source note | uspto-grants-2008_07 |
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