HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407170Generated: October 30, 2026
Ammonium Hydroxide → 4-Amino-3-chloro-5,6-difluoropicolinonitrile
https://huagongshe.com/reaction/407170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Chloro-4,5,6-trifluoro-2-pyridinecarbonitrile | HCID 70496890 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Amino-3-chloro-5,6-difluoropicolinonitrile | HCID 70497379 | 88.3% |
Reaction Steps
A solution of 3-chloro-4,5,6-trifluoropicolinonitrile (200 g) in EtOAc (3 L) was cooled to 10° C. To this was slowly added 14% aq NH4OH (1296 g) keeping the temperature between 18-23° C. The aqueous solution was separated from the organic solution. The organic phase was washed sequentially with a 50/50 solution of aqueous saturated NaCl and water (500 mL) and satd NaC1 solution (250 mL). The organic phase was concentrated under vacuum at 50° C. to about 500 mL volume as the product crystallized out. To this slurry was added heptane (1 L), and the mixture was concentrated under vacuum. The solids were collected by filtration. This solid was washed with pentane and dried under vacuum to give 4-amino-3-chloro-5,6-difluoropicolinonitrile (173.8 g, 90%, 99.6% purity) as a white crystalline solid: mp 190-191.5° C.; 13CNMR (101 MHz, DMSO-d6) δ 150.03 (dd, J=232.4, 12.5 Hz, C6), 144.29 (dd, J=11.4, 6.9 Hz, C4), 133.72 (dd, J=257.9, 30.8 Hz, C5), 122.14 (dd, J=19.6, 4.9 Hz, C2), 119.31 (s, C3), 114.25 (s, CN); 19F NMR (376 MHz, DMSO-d6) δ −91.24 (d, J=24.2 Hz), −154.97 (d, J=24.2 Hz); EIMS m/z 189 ([M]+). Anal. Calcd for C6H2C1F2N3: C, 38.02; H, 1.06; N, 22.17. Found: C. 37.91; H.1.00; 22.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754231B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-8def9b516cbc494ba2a05d5420fa4e3b |
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| Source note | uspto-grants-2014_06 |
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