HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178480237 | HCID 178480237 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazole | HCID 14032504 | 57.8% |
Reaction Steps
A solution of 0.52 g of paraformaldehyde, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole, 15 ml of ethanol and 0.34 ml of 5% aqueous sodium hydroxide was refluxed for 3 hrs. The ethanol was removed in vacuo and the residue diluted with water. The aqueous suspension was extracted with dichloromethane (2x, 50 ml) and the combined extracts were washed with water and dried over anhydrous magnesium sulfate. The dichloromethane was evaporated in vacuo to yield an oil, which crystallized upon standing. The solid was recrystallized twice from ethyl acetate to yield 1.3 g (57.8%) of product, mp 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04775761 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-b1cd6f65f9114292a63255529ebe0fe6 |
| Source note | uspto-grants-1988_10 |