HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 3-Allyloxycatechol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Allyloxy-2-ethoxy-1,3-benzodioxolane | HCID 69933774 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Allyloxycatechol | HCID 12208881 | — |
Reaction Steps
A solution of 38 (3.3 g, 15 mmol) and p-toluenesulfonic acid monohydrate (0.17 g, 0.9 mmol) in aqueous MeOH (21 mL, MeOH: H2O 20:1) was stirred at rt for 16 h, then neutralised by the addition of saturated NaHCO3 aq. and the methanol was removed in vacuo. The residue was extracted with t-BuOMe (3×) and the organic phase was dried (Na2SO4) and evaporated to dryness to give 39 compound (2.4 g, 95%) which was used as such in the next step:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198302B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-1d246614781d4ec18ae5839655e81a5a |
| Source note | uspto-grants-2012_06 |