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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985388Generated: October 28, 2026

Thiophenol → HCID 22506599, compound

https://huagongshe.com/reaction/985388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22506603HCID 22506603—
SolventDimethylformamideHCID 6228—
ProductHCID 22506599HCID 2250659923%

Reaction Steps

To a stirred solution of 4-diethoxyphosphoryl-1,7-bis(2-nitrobenzenesulfonyl)-1,4,7-triazacyclotetradecane (1.32 g, 1.87 mmol) and K2CO3 (654 mg, 4.73 mmol) in DMF (11 mL) under nitrogen was added dropwise a solution of thiophenol (0.15 mL, 1.46 mmol) in DMF (8 mL) over 1 h. The mixture was stirred for an additional 3 h and then concentrated in vacuo. The residue was partitioned between CHCl3 (50 mL) and H2O (25 mL). The aqueous phase was separated and extracted with CHCl3 (3×20 mL) and the combined organic extracts were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography on basic alumina (CHCl3 then 3% MeOH/CHCl3) to give the title compound as a yellow oil (178 mg, 23%): 1H NMR (CDCl3) δ 1.31 (t, 6H, J=7.0 Hz), 1.40-1.67 (m, 10H), 2.65 (m, 2H), 2.78 (m, 2H), 3.12 (m, 2H), 3.26-3.37 (m, 4H), 3.48 (m, 2H), 3.97-4.09 (m, 4H), 7.61 (m, 1H), 7.68 (m, 2H), 8.06 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872714B1
Source datasetuspto-grants-2005_03
ORD IDord-ff56fa261a9f4ab4bf3c1427a7e5607b
Source noteuspto-grants-2005_03