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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584096Generated: October 30, 2026

p-Anisoyl chloride → HCID 5097621, compound

https://huagongshe.com/reaction/584096

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 178418616HCID 178418616—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5097621HCID 5097621—

Reaction Steps

Following the general procedure described above, reaction of p-anisoyl chloride (4.70 g, 30.0 mmol) with 2-mercaptopyridine (3.33 g, 30.0 mmol) in THF (30 mL) for 30 min at room temperature afforded pale yellow solid after precipitation (6.70 g, 91%): mp 73° C.; 1H NMR δ 3.88 (s, 3H), 6.93-7.00 (m, 2H), 7.30-7.34 (m, 1H), 7.70-7.74 (m, 2H), 7.75-7.80 (m, 1H), 7.97-8.02 (m, 1H), 8.64-8.69 (m, 1H); Anal. Calcd for C13H11NO2S: C, 63.65; H, 4.52; N, 5.71. Found: C, 63.78; H, 4.59; N, 5.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924375B2
Source datasetuspto-grants-2005_08
ORD IDord-d54c4a2a555140b1992fe756bbaf5f63
Source noteuspto-grants-2005_08