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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377174Generated: October 26, 2026

Acetone → HCID 21221128, compound

https://huagongshe.com/reaction/1377174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium IodideHCID 5238—
ReactantToluene, alpha-chloro-2,3,4-trimethoxy-HCID 97491—
SolventDiethyl EtherHCID 3283—
ProductHCID 21221128HCID 21221128—

Reaction Steps

46.64 g (215.2 mmol) of 2,3,4-trimethoxybenzyl chloride in 466 ml of abs. acetone are treated with 156.7 g (4.86 equivalents) of sodium iodide, and this mixture is stirred at RT for 2.75 h while excluding light. The reaction mixture is treated with approximately 3 l of (cold) ether, and the organic phase is washed once with 10 sodium thiophosphate solution and twice with saline (both kinds of solutions being cold). The combined aqueous phases are reextracted with ether. The combined organic phases are dried over Na2SO4 and evaporated on a RE at approximately 30° C. The residue, which is the desired title compound, is dried again under HV and subjected to further processing as a crude product. 1H-NMR (200 MHz, CDCl3): 7.03 and 6.59 (each d; each 1H); 4.47 (s, 2H); 4.05, 3.85 and 3.84 (each s, each 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663200
Source datasetuspto-grants-1997_09
ORD IDord-650d00b895b846988f0a51b96bfbbc18
Source noteuspto-grants-1997_09