HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900560Generated: October 29, 2026
Sodium Hydroxide → 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]benzoic acid
https://huagongshe.com/reaction/900560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid methyl ester | HCID 86595067 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]benzoic acid | HCID 59697064 | 50% |
Reaction Steps
A 6M aq. solution of NaOH (15 ml) was added to a stirred solution of 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid methyl ester. (9.06 g, 30 mmol) in MeOH (350 ml) at rt. The reaction solution was heated to reflux for 3 hours. The reaction stayed a mixture and did not turn clear. HPLC and LCMS indicated that the reaction was forming side products. The reaction was cooled to rt and some MeOH (˜200 ml) was removed by evaporation under reduced pressure. Water (400 ml) was added to the mixture. Conc. HCl was added dropwise to the stirred solution until acidic by pH paper (pH2). The yellow precipitate that formed was collected by suction filtration. The solid was washed with water (3×20 ml) and hexane (2×20 ml) to give the crude product. HPLC indicated that there was approximately 40% product in the mixture. The crude reaction product was purified by flash chromatography using EtOAc (8-10%)/hexane as eluant. The pure fractions were evaporated and dried in vacuo to give 4.2 g of product 3 in 50% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358359B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-7b335ecf6d60411d90b4b54ba4dd3c12 |
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| Source note | uspto-grants-2008_04 |
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