HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3,5-Dihydroxy-4-((E)-3-phenyl-allyl)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3,5-Bis-methoxymethoxy-4-((E)-3-phenyl-allyl)-benzoic acid | HCID 66756041 | — |
| Product | 3,5-Dihydroxy-4-((E)-3-phenyl-allyl)-benzoic acid methyl ester | HCID 58146227 | 73% |
Reaction Steps
To a solution of 3,5-bis-methoxymethoxy-4-((E)-3-phenyl-allyl)-benzoic acid (220g) (18 g, 0.05 mol) in MeOH (300 mL) was added catalytic amount of conc. H2SO4 (3 mL) in one portion. The mixture was refluxed overnight. The solution was concentrated. The residue was dissolved in CH2Cl2 (75 mL) and washed with sat. NaHCO3 (25 mL). The organic layers were dried and concentrated to give a brown solid (12 g, 73% yield). 1H NMR (400 MHz, CDCl3): δ 9.63 (s, 2H), 7.11˜7.34 (m, 5H), 6.93 (s, 2H), 6.32 (s, 2H), 3.77 (s, 3H), 3.42 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119624B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-6dfa7d853e4a4442a6a9ed42508f3495 |
| Source note | uspto-grants-2012_02 |