HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407834Generated: November 1, 2026
Ethanol → 2-Chloro-6-methyl-5-nitronicotinonitrile
https://huagongshe.com/reaction/2407834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 178433464 | HCID 178433464 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 2-Chloro-6-methyl-5-nitronicotinonitrile | HCID 13240382 | 37.9% |
Reaction Steps
A suspension of the compound prepared in Example 442 (5.00 g) and phosphorus pentachloride (6.97 g) in phosphorus oxychloride (25 mL) was stirred and heated in an oil bath set to 110° C. for 30 minutes. The resulting solution was cooled to ambient temperature and concentrated. The residual liquid was cooled in an ice bath, whereupon a solid formed. This solid was carefully treated with 50% aqueous ethanol (10 mL), and then the mixture was stirred and heated in the 110° C. oil bath for 5 minutes. This redissolved the solid, and then the flask was again placed in the ice bath. The solid reappeared on cooling, and it was collected by filtration, washed with water, and air-dried. The solid was then recrystallized by stirring it with methanol (20 mL), and heating to boiling until all solid dissolved. On cooling to ambient temperature crystallization began, and the mixture was stored in the refrigerator overnight. The crystals were collected by filtration, washed with cold methanol, and dried under vacuum to provide the title compound (2.09 g) with the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809538B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-18aa4efe2ae64d1d881eedb291115d5d |
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| Source note | uspto-grants-2014_08 |
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