HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519274Generated: November 4, 2026
Sodium Hydroxide → 4-[4-(3-Chloro-4-fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid
https://huagongshe.com/reaction/1519274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[4-(3-Chloro-4-fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester | HCID 86679842 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-[4-(3-Chloro-4-fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid | HCID 71536628 | 61.9% |
Reaction Steps
Sodium hydroxide (100 mg, 2.5 mmol) was added to a suspension of 4-[4-(3-chloro-4-fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid methyl ester (100 mg) in a mixture of water (2 mL) and dioxane (4 mL). The reaction mixture was stirred at 50° C. for 2 h. An additional portion of water (2 mL) was added and the reaction mixture was stirred at 50° C. for a further 2 h. The reaction mixture was evaporated to dryness and water (5 mL) was added. The mixture was filtered and the filtrate was made acidic to pH 3-4 by the addition of concentrated HCl. The precipitate was collected by filtration and dried to give 4-[4-(3-chloro-4-fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid (60 mg, 41% for two steps). 1H NMR (300 MHz, DMSO-d6) δ 13.18 (br s, 1H), 8.56 (s, 1H), 8.39 (s, 1H), 8.27 (d, J=8.3 Hz, 1H), 8.08-8.16 (m, 2H), 7.79 (t, J=7.4 Hz, 1H), 7.66 (t, J=7.9 Hz, 1H), 7.41-7.58 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073881B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-8f2bbfd22f2f4a7d9e5fda90c312c697 |
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| Source note | uspto-grants-2015_07 |
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