HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250403Generated: October 25, 2026
Phenol → 4-Hydroxy-1-phenoxy-isoquinoline-3-carboxylic acid butyl ester
https://huagongshe.com/reaction/250403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester | HCID 86014502 | — |
| Product | 4-Hydroxy-1-phenoxy-isoquinoline-3-carboxylic acid butyl ester | HCID 66712944 | 38.5% |
Reaction Steps
A mixture of 1.399 g of 1-Chloro-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester (5 mmol) and 2.86 g of phenol was heated at 145° C. to 150° C. for 24 h. After cooling to ambient temperature the mixture was suspended in 50 ml of aqueous 2N NaOH and the mixture was extracted with 4×25 ml of ethyl acetate. The combined organic phases were washed with 3×25 ml of aqueous 2N NaOH, 50 ml of brine, dried over MgSO4, and evaporared in vacuo. The residue was purified by flash column chromatography on silica gel eluting with hexanes:ethyl acetate (9:1) and (95:5). 0.650 g of the title compound were obtained; 1H NMR (CDCl3): δ=11.52 (s, 1H), 8.32 to 8.39 (m, 2H), 7.72 to 7.86 (m, 2H), 7.13 to 7.42 (m, 5H), 4.31 (t, 2H), 1.69 (m, 2H), 1.37 (m, 2H), 0.93 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863292B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ebcb266977f045b7bd7a50b9296c232c |
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| Source note | uspto-grants-2011_01 |
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