HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 22-(2-Hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12824096 | HCID 12824096 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 22-(2-Hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid | HCID 12824074 | — |
Reaction Steps
In 15 ml of methanol is dissolved 300 mg of methyl 22-(2-hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoate followed by addition of 20 ml of a 14% aqueous solution of sodium hydroxide. The mixture is stirred at 50°-60° C. for 1.5 hours. The reaction mixture is made acidic with 3N--HCl and extracted with ethyl acetate. The extract is washed with water and, after drying, the solvent is distilled off under reduced pressure. The residue is recrystallized from methanol to obtain 22-(2-hydroxy-3,4-dimethoxy-6-methylphenyl)docosanoic acid (IV:n=21), m.p. 67° C.-68° C. NMR(δ, in deuteriochloroform): 1.27(38H,b,CH2), 2.24(3H,s,nuclear CH3), 2.28-2.56(4H,m,CH2COO, nuclear CH2), 3.80(3H,s,OCH3), 3.84(3H,s,OCH3), 6.24(1H,s, nuclear H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04495104 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-9fdae08b440143c3ab3bdc4481e978e2 |
| Source note | uspto-grants-1985_01 |