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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817135Generated: October 30, 2026

Acetyl chloride → HCID 86635767, compound

https://huagongshe.com/reaction/1817135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 66912535HCID 66912535—
ProductHCID 86635767HCID 8663576768%

Reaction Steps

To a solution of acetyl 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-(acetamido)-4-methoxybenzylsulfone in 68% yield. M.p. 220-223° C. NMR (DMSO-d6) δ 2.02(s, 2H), 3.84(s, 3H), 3.86(s, 6H), 3.88(s, 3H), 4.22 (s, 2H), 6.08(s, 2H), 7.09-7.12(d, 1H vinylic), 6.88-7.86(m, aromatic), 8.35(s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598232B2
Source datasetuspto-grants-2009_10
ORD IDord-4a6f1ee3eb014fe597eccb106cc0eb4b
Source noteuspto-grants-2009_10