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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817131Generated: October 30, 2026

Benzoyl chloride → HCID 86598613, compound

https://huagongshe.com/reaction/1817131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 66912535HCID 66912535—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86598613HCID 8659861376%

Reaction Steps

To a solution of benzoyl 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 up 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-benzamido-4-methoxybenzylsulfone in 76% yield. m.p. 163-166° C. NMR (DMSO-d6) δ 3.82(s, 3H), 3.83(s, 6H), 3.86(s, 3H), 4.2(s, 2H), 6.14(s, 2H), 7.10-7.18(d,1 H vinylic), 7.00-7.86(m, aromatic), 8.90(s,1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598232B2
Source datasetuspto-grants-2009_10
ORD IDord-30de60293506450aa7e63bed3ac14bbd
Source noteuspto-grants-2009_10