HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 20495945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 13187542 | HCID 13187542 | — |
| Product | HCID 20495945 | HCID 20495945 | 99% |
Reaction Steps
By the same procedure as described in Reference Example 58, 2,3-dimethoxy-5-methyl-6-(tetrahydrofur-2-yl)-1,4-benzohydroquinone (27 g, 0.106 mole) was methylated with methyl iodide, thereby being derived into 1,2,3,4-tetramethoxy-5-methyl-6-(tetrahydrofur-2-yl)benzene (28.5 g, 98%, bp1.0 135° to 138° C.). The catalytic reduction of the compound afforded 1,2,3,4-tetramethoxy-5-methyl-6-(4-hydroxybutyl)benzene (28.2 g, 99%, oily substance).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04393075 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-33f482d33825431a97e9e86ebf99486b |
| Source note | uspto-grants-1983_07 |