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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | 1H-Indazole-6-carbaldehyde | HCID 18538368 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Methoxybenzyl)-1H-indazole-6-carbaldehyde | HCID 86681512 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921545B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-82e4ac875b3b4dcb90f880731c57ad92 |
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| Source note | uspto-grants-2014_12 |
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