HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461584Generated: October 26, 2026
Water → 2-Chloro-6-(4-isothiocyanatophenoxy)pyridine
https://huagongshe.com/reaction/461584
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Benzenamine, 4-[(6-chloro-2-pyridinyl)oxy]- | HCID 13980869 | — |
| Product | 2-Chloro-6-(4-isothiocyanatophenoxy)pyridine | HCID 21391418 | — |
Reaction Steps
Thiophosgene (10.5 grams; 0.091 mole) was added to an agitated solution of water (170 ml.) and dimethoxyethane (25 ml.) 4-((6-Chloro-2-pyridinyl)oxy)benzenamine (20 grams; 0.0906 mole) was added in small portions (the dimethoxyethane aids in suspending the amine in the aqueous thiophosgene solution) to the stirred thiophosgene solution over a 20 minute period. The reactive temperature during the addition was 25°-30° C. Following the addition of the amine reactant, the reaction mixture was filtered to recover the product precipitate which formed during the reaction. The precipitate was then dissolved in boiling hexane and the resulting solution dried and cooled to give the desired 4-((6-chloro-2-pyridinyl)oxy)phenyl isothiocyanate product as a light yellow crystalline solid having a melting point of 59°-62° C. The product was found to have carbon, hydrogen, nitrogen, chlorine and sulfur contents of 55.5, 2.3, 10.9, 13.36 and 12.34 percent, respectively, as compared with the theoretical contents of 54.82, 2.69, 10.66, 13.5 and 12.2 percent, respectively, calculated for the named structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04063928 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-341016cd6e684623b5434637201a3a7b |
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| Source note | uspto-grants-1977_12 |
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