HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530836Generated: October 30, 2026
Trityl chloride → HCID 67984870, compound
https://huagongshe.com/reaction/530836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178468688 | HCID 178468688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67984870 | HCID 67984870 | 97.8% |
Reaction Steps
To a suspension of ethyl 3-bromo-1H-indazole-5-carboxylate (10.72 gm, 0.04 mol) in 160 mL of THF was added NaH (2.8 g, 0.068 mol) portionwise at 5-10 C under ice/water bath. The solution was stirred for 15 minutes further until no more bubbling. Tritylchloride (14 g, 0.05 mol) was added in several portions. After the addition, the cooling bath was removed and the orange suspension was stirred at room temperature for overnight. The reaction mixture was poured slowly into 100 mL of saturated NH4Cl with stirring and 100 mL EtOAc. The layers were separated and the aqueous phase extracted with Ethyl acetate (2 L×2). The combined organic layers were washed with water (100 mL), brine (100 mL), dried over Na2SO4, filter and concentrated. The solid was triturated with hexane (100 mL), filtered and washed with hexane and dried under vacuum to give 20 gram product as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09351965B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7b8ddf125196471db000119b2b952816 |
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| Source note | uspto-grants-2016_05 |
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