Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867676Generated: October 25, 2026

Formaldehyde → 1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazole

https://huagongshe.com/reaction/867676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178480237HCID 178480237—
SolventEthanolHCID 702—
Product1-Hydroxymethyl-3-(1-methyl-4-piperidinyl)-1H-indazoleHCID 1403250457.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775761
Source datasetuspto-grants-1988_10
ORD IDord-b1cd6f65f9114292a63255529ebe0fe6
Source noteuspto-grants-1988_10