HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545490Generated: October 29, 2026
Acetic Anhydride → HCID 11473695, compound
https://huagongshe.com/reaction/545490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 67200299 | HCID 67200299 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11473695 | HCID 11473695 | 69% |
Reaction Steps
To a solution of 6-(benzylamino)-methyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (112 mg, 0.34 mmol), NMM (0.12 mL, 1.09 mmol) and DMAP (10 mg, 0.08 mmol) in anhydrous dichloromethane (5 mL) at 0° C. was added acetic anhydride (48 μL, 0.51 mmol). The reaction mixture was allowed to warm to rt. After the reaction was complete, 5 mL of saturated NaHCO3 was added. The organic layer was separated, washed with 5 mL of water and then concentrated. After drying under high vacuum, the residue was dissolved in anhydrous MeOH (6 mL) and hydroxylamine hydrochloride (90 mg, 1.30 mmol) was added, followed by the addition of NaOMe solution (4.37 M in MeOH, 0.57 mL, 2.5 mmol). The mixture was allowed to stir at rt till the reaction was complete. The reaction mixture was concentrated and the residue was dissolved in a minimal amount of water. The obtained solution was acidified with 2N HCl to pH≈8. The solid formed was filtered, washed with water, collected and purified by flash column chromatography to give 6-[(acetyl-benzyl-amino)-methyl]-benzo[b]thiophene-2-carboxylic acid hydroxyamide as a pale solid (83.3 mg, 69%). 1H NMR (DMSO-d6, 200 MHz) δ 11.47 (brs, 1H), 9.30 (brs, 1H), 7.98-7.74 (m, 3H), 7.44-7.10 (m, 6H), 4.65-4.40 (m, 4H), 2.12 (s, 3H). MS (EI): cal'd 355.1 (MH+), exp 355.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935724B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-fd660dc3438142429115dc7c8715b5db |
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| Source note | uspto-grants-2011_05 |
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