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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817132Generated: October 31, 2026

4-Nitrobenzoyl chloride → HCID 86598615, compound

https://huagongshe.com/reaction/1817132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHCID 66912535HCID 66912535—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86598615HCID 8659861572%

Reaction Steps

To a solution of 4-nitrobenzoyl chloride (10 mmol) in tetrahydrofuran (40 mL) was added dropwise a solution of 2,4,6-trimethoxystyryl-3-amino-4-methoxybenzylsulfone (10 mmol) in tetrahydrofuran. The solution was stirred overnight and the completion of the reaction was monitored by TLC. The solvent was removed and the residue was taken in dichloromethane and washed with water. The organic layer was dried over anhydrous sodium sulfate and evaporated to give (E)-2,4,6-trimethoxystyryl-3-(4-nitrobenzamido)-4-methoxybenzylsulfone in 72% yield. m.p. 206-208° C. NMR (DMSO-d6) δ 3.80(s, 3H), 3.81(s, 6H), 3.83(s, 3H), 4.18(s, 2H), 6.08(s, 2H), 7.14-7.23(d, 1H vinylic), 6.97-7.86(m, aromatic), 9.05(s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598232B2
Source datasetuspto-grants-2009_10
ORD IDord-bae92dcb78ac4aedaae89e7b263fa1cf
Source noteuspto-grants-2009_10