HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646229Generated: October 31, 2026
2,4,6-Trimethylpyridine → HCID 53823294, compound
https://huagongshe.com/reaction/1646229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 54260281 | HCID 54260281 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53823294 | HCID 53823294 | — |
Reaction Steps
Under a current of argon, a solution of 1.50 g of 4-methoxymethoxy-3-nitrocinnamyl alcohol in 15 ml of dimethyl formamide and 292 mg of anhydrous lithium chloride and 0.9 ml of 2,4,6-collidine added thereto as kept cooled with ice were stirred for 10 minutes and the produced mixture and 0.5 ml of methanesulfonyl chloride added as kept cooled with ice were stirred for four hours. The resultant reaction mixture was combined with water and extracted from ethyl acetate. The consequently separated organic layer was washed with saturated saline solution and dried with anhydrous sodium sulfate. By concentrating the residue from drying under a vacuum, 1.62 g of 4-methoxymethoxy-3-nitrocinnamyl chloride was obtained in the form of a colorless oily substance. This product was put to use in its unpurified form in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05179105 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-d743d0320870420886667367fe6a89f1 |
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| Source note | uspto-grants-1993_01 |
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