HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35537Generated: October 28, 2026
Acetic Acid → 3-Acetoxy-2-(4-methoxyphenyl)-6-azabenzo[b]thiophene
https://huagongshe.com/reaction/35537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-(4-methoxyphenyl)methylthiopyridine-4-carboxylate | HCID 86742397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Acetoxy-2-(4-methoxyphenyl)-6-azabenzo[b]thiophene | HCID 14277638 | 48% |
Reaction Steps
A solution of 0.200 g (.69 mmol) of methyl 3-(4-methoxyphenyl)methylthiopyridine-4-carboxylate in 2 mL of dry tetrahydrofuran was added to a suspension of 83 mg (2.1 mmol) of 60% dispersion of sodium hydride in 2 mL of dry N,N-dimethylformamide. The mixture was stirred at room temperature for 3 hours, then poured onto ice water and acidified with glacial acetic acid. The solid material (product) was collected by filtration and the filtrate was extracted with ethyl acetate. The ethyl acetate extract was dried, concentrated and combined with the solid precipitate that had been collected. This material was heated at reflux with 100 mg sodium acetate in 2 mL of acetic anhydride for 2 hours, then was partitioned between ethyl acetate and water. The aqueous layer was washed with two portions of ethyl acetate and the combined extracts were dried and concentrated. The residue was crystallized from methanol to afford 100 mg (48%) of white crystalline material, m.p. 141-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04767766 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-8f4e2abc12d546a996287a3be0ac6dcc |
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| Source note | uspto-grants-1988_08 |
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