HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 23454861, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 23454838 | HCID 23454838 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23454861 | HCID 23454861 | 74.9% |
Reaction Steps
A mixture of 14.3 g of 1-(2,3,4-trimethoxyphenyl)-2-methyl-2-nitropropanol, 11.9 g of thionyl chloride and 150 ml of anhydrous benzene is refluxed for 3.5 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (yellow oil) is purified by silica gel chromatography (Solvent: n-hexane-ethyl acetate (10:1). 11.4 g of 1-(2,3,4-trimethoxyphenyl)-1-chloro-2-methyl-2-nitropropane are thereby obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04276304 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-2184a44bdcbb4a4baeb9ae7ae6f0c3a1 |
| Source note | uspto-grants-1981_06 |