Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410336Generated: November 2, 2026

4-Methyloxybenzyl chloride → 1-(4-Methoxybenzyl)-1H-indazole-6-carbaldehyde

https://huagongshe.com/reaction/1410336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant1H-Indazole-6-carbaldehydeHCID 18538368—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product1-(4-Methoxybenzyl)-1H-indazole-6-carbaldehydeHCID 8668151272%

Reaction Steps

To a solution of 1H-indazole-6-carbaldehyde (1.5 g, 10.3 mmol) in DMF (10 mL) at 0° C. was added KOtBu (1.4 g, 12.4 mmol) and let stir for 10 min. PMBCl (1.7 mL, 12.4 mmol) was then added and let slowly warm to room temperature. After 1.5 h the reaction was quenched with NH4Cl. The product was extracted with Et2O and the organic layers was washed brine and then dried over MgSO4. The solvent was removed and the crude material (mixture of N1 and N2 isomers) was dried under high vacuum. To the resulting residue was added PMBCl (0.70 mL, 5.15 mmol) and the mixture heated to 170° C. for 2.5 h. Cooled to room temperature and purified residue using Biotage Isolera (silica gel, 20-50% EtOAc in hexane) which gave the title compound (1.97 g, 72%). 1H NMR (400 MHz, CDCl3) δ 10.09 (s, 1H), 8.12 (s, 1H), 7.91 (s, 1H), 7.85 (d, J=8.4 Hz, 1H), 7.67 (d, J=8.4 Hz, 1H), 7.21 (d, J=8.5 Hz, 2H), 6.85 (d, J=8.6 Hz, 2H), 5.62 (s, 2H), 3.77 (s, 3H); MS ESI 266.9 [M+H]+, calcd for [C16H14N2O2+H]+ 267.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921545B2
Source datasetuspto-grants-2014_12
ORD IDord-82e4ac875b3b4dcb90f880731c57ad92
Source noteuspto-grants-2014_12