Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530836Generated: October 30, 2026

Trityl chloride → HCID 67984870, compound

https://huagongshe.com/reaction/530836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178468688HCID 178468688—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67984870HCID 6798487097.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351965B2
Source datasetuspto-grants-2016_05
ORD IDord-7b8ddf125196471db000119b2b952816
Source noteuspto-grants-2016_05