HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39333Generated: October 28, 2026
Sodium Hydroxide → 6-Hydroxy[1]benzofuro[3,2-c]pyridine-9-carbaldehyde-2-oxide
https://huagongshe.com/reaction/39333
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(Cyclopentyloxy)[1]benzofuro[3,2-c]pyridine-9-carbaldehyde 2-oxide | HCID 86643119 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Hydroxy[1]benzofuro[3,2-c]pyridine-9-carbaldehyde-2-oxide | HCID 25118278 | 80% |
Reaction Steps
A well stirred suspension of 6-(cyclopentyloxy)[1]benzofuro[3,2-c]pyridine-9-carbaldehyde 2-oxide (200 mg, 0.671 mmol) in 48% aqueous hydrobromic acid (10 mL) was heated to 70-80° C. for 2-3 hours. The reaction mixture was cooled to room temperature and diluted with water (50 mL) and was made alkaline (pH=9-10) by means of a 10% aqueous solution of sodium hydroxide. It was then washed with ethyl acetate (2×25 mL). The aqueous layer was then acidified with acetic acid (pH=4-5) and stirred at 10-15° C. for 30-40 minutes. The solid obtained was filtered and dried to afford 6-hydroxy[1]benzofuro[3,2-c]pyridine-9-carbaldehyde-2-oxide (Yield=80-90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524905B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-126cb5487f434bd3905237bb52f0569b |
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| Source note | uspto-grants-2013_09 |
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