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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220202Generated: October 31, 2026

Acetic Anhydride → HCID 68892581, compound

https://huagongshe.com/reaction/2220202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 69196263HCID 69196263—
SolventTolueneHCID 1140—
ProductHCID 68892581HCID 6889258172%

Reaction Steps

To a mixture of 8-Bromo-2-chloro-5,6-dihydro-dibenzo[b,f]azocine (0.8 g, 2.5 mmole) in toluene (10 mL) was added acetic anhydride (1.2 mL, 12.5 mmole) and N,N-dimethylaminopyridine (1.51 g, 12.5 mmole). The reaction mixture was refluxed for 2 hours, concentrated and purified by flash chromatography over silica gel eluting with 30% ethyl acetate/hexane to give 1-(8-Bromo-2-chloro-6H-dibenzo[b,f]azocin-5-yl)-ethanone (0.65 g, 72%). 1HNMR (CDCl3) δ7.32 (d, 1H, J=1.76 Hz), 7.23 (dd, 1H, J=7.70, 1.76 Hz), 7.19 (m, 2H), 7.06 (d, 1H, J=8.80 Hz), 6.91 (d, 1H, J=8.36 Hz), 6.68 (d, 1H, J=13.16 Hz), 6.47 (d, 1H, J=12.76 Hz), 5.42 (d, 1H, J=14.96 Hz), 4.08 (d, 1H, J=15.36 Hz), 1.68 (s, 3H). HPLC Rt=4.05 min. m/z=362 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417040B2
Source datasetuspto-grants-2008_08
ORD IDord-f2ba1101139047dfa1e803a4ea50a76c
Source noteuspto-grants-2008_08