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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722787Generated: October 30, 2026

Azobisisobutyronitrile → HCID 20728721, compound

https://huagongshe.com/reaction/722787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 20728726HCID 20728726—
ReactantHCID 178418634HCID 178418634—
SolventBenzeneHCID 241—
ProductHCID 20728721HCID 2072872160%

Reaction Steps

To a solution of 2-ethenyl-6-[4-(methoxycarbonyl)phenyl]methoxy-benzoic acid, methyl ester (0.71 g, 2.18 mmol) in benzene (10 mL) was added thioacetic acid (1.80 mL, 25.2 mmol) followed by AIBN (37 mg, 0.23 mmol). After nitrogen was bubbled through the solution for 30 min, the solution was heated at reflux for 4 h. The reaction was allowed to cool to rt and saturated NaHCO3 (20 mL) was added. The mixture was extracted with EtOAc (3×20 mL). The combined organic extracts were washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (1:10 EtOAc/hexanes) to give 2-[2-(acetylthio)ethyl]-6-[4-(methoxycarbonyl)phenyl]methoxy-benzoic acid, methyl ester (0.50 g, 60%) as a clear oil: 1H NMR (CDCl3) δ 2.34 (s, 3H), 2.85–2.82 (m, 2H), 3.07–3.10 (m, 2H), 3.92 (s, 3H), 3.94 (s, 3H), 5.16 (s, 2H), 6.81 (d, J =8.2 Hz, 1H), 6.92 (d, J =7.7 Hz, 1H), 7.28 (t, J=8.2 Hz, 1H), 7.46 (d, J=8.3 Hz, 2H), 8.04 (d, J=8.3 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138543B2
Source datasetuspto-grants-2006_11
ORD IDord-89fc710a46f148fbb7146d3b5c750a05
Source noteuspto-grants-2006_11