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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054587Generated: November 1, 2026

Acetic Anhydride → HCID 16762877, compound

https://huagongshe.com/reaction/1054587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 16764930HCID 16764930—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 16762877HCID 1676287767.4%

Reaction Steps

To a solution of 2-(4-bromophenoxy)ethanamine (500 mg, 2.3 mmol) in CH2Cl2 (20 mL) was added triethylamine (700 mg, 6.9 mmol) and acetic anhydride (470 mg, 4.6 mmol). The reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated in vacuo to give a yellow residue. The crude product was diluted with ethyl acetate (20 mL), washed with 1 N HCl followed by saturated sodium bicarbonate, dried over sodium sulfate and concentrated in vacuo to give N-[2-(4-bromophenoxy)ethyl]acetamide (400 mg, 67%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.39 (d, 2 H), 6.76 (d, 2 H), δ 5.89 (m, 1 H), 4.00 (m, 2 H), 3.67 (m, 2 H), δ 2.01 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-85b5baac6ab342df8b78fee018a57fb4
Source noteuspto-grants-2016_07