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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545490Generated: October 29, 2026

Acetic Anhydride → HCID 11473695, compound

https://huagongshe.com/reaction/545490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-MethylmorpholineHCID 7972—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 67200299HCID 67200299—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 11473695HCID 1147369569%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935724B2
Source datasetuspto-grants-2011_05
ORD IDord-fd660dc3438142429115dc7c8715b5db
Source noteuspto-grants-2011_05