HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615266Generated: November 2, 2026
2-Chloromethyl 2-(trimethylsilyl)ethyl ether → HCID 86651953, compound
https://huagongshe.com/reaction/1615266
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Reactant | 4-bromo-1H-indazole-6-carbaldehyde | HCID 59635585 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 86651953 | HCID 86651953 | 82% |
Reaction Steps
To a solution of 4-bromo-1H-indazole-6-carbaldehyde (225 mg, 1 mmol) in CH2Cl2 (10 mL) and aqueous KOH (2 mL, 50% wt) at 0° C. was added TBAB (3 mg, 0.01 mmol) and SEMCl (200 mg, 1.2 mmol). The mixture was stirred at 0° C. for 4 h, warmed to rt and extracted with ethyl acetate (100 mL). The organic phase was washed with water (2×10 mL) and brine (10 mL), dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography (1:1 EtOAc/Hex) to give the title compound as a pale yellow solid (280 mg, 82%). 1H NMR (400 MHz, CD3OD) δ 10.02 (s, 1H), 8.21-8.19 (m, 2H), 7.80 (s, 1H), 5.78 (s, 2H), 3.70-3.65 (m, 2H), 0.95-0.92 (m, 2H), −0.05 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765748B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-9eb12490dad24e6580fa33006e17dcd0 |
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| Source note | uspto-grants-2014_07 |
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