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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67078Generated: October 30, 2026

Sodium borohydride → 2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-hydroxy-2-phenylethyl)-4-piperidinyl)-

https://huagongshe.com/reaction/67078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12797991HCID 12797991—
SolventMethanolHCID 887—
Product2(1H)-Quinazolinone, 3,4-dihydro-3-(1-(2-hydroxy-2-phenylethyl)-4-piperidinyl)-HCID 306138663.5%

Reaction Steps

In this example, 2.30 g of 1-benzoylmethyl-4-[3,4-dihydro-2(1H)-quinazolinon-3-yl]-piperidine and 100 ml of methanol are mixed and stirred at room temperature. To the stirred mixture, 1.5 g of sodium borohydride is added over a period of 5 hours. Then, the mixture is stirred overnight at room temperature. The white crystals deposited are separated by filtration, successively washed with methanol and water and dried to obtain 2.06 g of a crude product. The crude product is recrystallized from a mixed solvent of chloroform and ethanol to obtain 1.47 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344948
Source datasetuspto-grants-1982_08
ORD IDord-3b60b47fb05a42fd8732d7861d2d1c48
Source noteuspto-grants-1982_08