HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 19011014, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19010982 | HCID 19010982 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19011014 | HCID 19011014 | 68% |
Reaction Steps
1,5,6,7,8,8a-Hexahydro-7,8-(dimethylmethylenedioxy)-6-methoxymethoxy-3H-2-benzopyran-3-ol (3.8 mg) was dissolved in 0.6 ml of dry methanol, and a catalytic amount of p-toluenesulfonic acid was added at room temperature. After the mixture was stirred at room temperature for 2 hours, triethylamine was added, and concentrated with water cooling under reduced pressure. The obtained residue was purified through a short silica gel column to provide 1.3 mg of 1,5,6,7,8,8a-hexahydro-6-methoxymethoxy-3-methoxy-3H-2-benzopyran-7,8-diol having the following properties (yield 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05334740 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-3f0a2b9486e74f76be7a03232ba74bf8 |
| Source note | uspto-grants-1994_08 |