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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212791Generated: November 2, 2026

Tetrahydrofuran → HCID 21954381, compound

https://huagongshe.com/reaction/2212791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21954379HCID 21954379—
SolventMethanolHCID 887—
ProductHCID 21954381HCID 2195438198.4%

Reaction Steps

A 100-ml Kolben equipped with a stirrer and a condenser was charged under a nitrogen stream with 18 g (15.6 mmol) of 4-(carbazol-9-yl)-4′-(3-formylcarbazol-9-yl)-biphenyl prepared above and 800 ml of tetrahydrofuran. Sodium tetrahydroborate (0.65 g, 17.2 mmol) was introduced at room temperature into the above mixture, and the mixture was stirred for one hr. Thereafter, 160 ml of methanol was introduced into the reaction solution, and the mixture was stirred for 3 hr. The solvent was distilled off, and the residue was dissolved in 500 ml of toluene. The solution was washed with water, and the solvent was then distilled off to give 4-(carbazol-9-yl)-4′-(3-hydroxymethylcarbazol-9-yl)-biphenyl (7.9 g, yield 98.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105258B2
Source datasetuspto-grants-2006_09
ORD IDord-32f79305be7b43faa997e66eb2363e0b
Source noteuspto-grants-2006_09