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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582672Generated: October 30, 2026

p-Chlorothiophenol → HCID 67597008, compound

https://huagongshe.com/reaction/582672

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantHCID 86751471HCID 86751471—
SolventHexaneHCID 8058—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 67597008HCID 6759700877.7%

Reaction Steps

To a solution 11-chloro-5-methylbenzofuro[3,2b]quinoline trifluoromethanesulfonate from Example 56 (65 mg, 0.156 mmol) in 2-ethoxyethanol (5 ml) was added 4-chlorothiophenol (23 mg, 0.156 mmol) causing the reaction mixture to became a bright yellow. After 5-7 min, TLC showed the disappearance of the starting material. The reaction mixture was cooled to room temperature, diluted with hexane (100 mL), cooled below room temperature, filtered and dried to afford 50 mg (63%) of the title compound, mp 150-151° C.; 1H NMR (CDCl3) δ8.71 (d, 1H, J=7.6), 8.60 (s, 2H), 8.23 (s, 1H), 7.96 (s, 1H), 7.86 (t, 1H, J=6.8), 7.64 (m, 2H), 7.44-7.37 (m, 4H), 5.06 (s, 3H); 13C NMR (CDCl3) δ 159.65, 146.54, 140.91, 139.53, 137.16, 136.95, 136.13, 135.33, 25 135.10, 130.24, 129.26, 127.46, 126.74, 126.65, 126,48, 126.08, 119.23, 116.29, 113.54, 41.25; MS (FAB, m/z) 376 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925647
Source datasetuspto-grants-1999_07
ORD IDord-2ac1e5ee89d44f429bfab4006949a1c2
Source noteuspto-grants-1999_07