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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576322Generated: November 2, 2026

Benzyl Bromide → HCID 21511899, compound

https://huagongshe.com/reaction/1576322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21511885HCID 21511885—
ProductHCID 21511899HCID 2151189983.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 0.93 g of 9-nitro-2,3,6,10b-tetrahydro-10b-phenyl-5H-oxazolo[3,2-C]quinazolin-5-one in 10 ml. of dimethylfomamide was added 0.18 g of 52.9% sodium hydride. The mixture was stirred with heating at 60°C for 1 hr. then, 0.68 g of benzyl bromide was added thereto. The resulting mixture was heated at 100°C for 4 hours. After cooling, the reaction mixture was poured into 50 ml. of water and the resulting precipitates were collected by filtration, washed with water and dried. The crude product was recrystallized from a mixture of methanol and carbon tetrachloride to give 1.0 g of 9-nitro-2,3,6,10b-tetrahydro-6-benzyl-10b-phenyl-5H-oxazolo[3,2-C]quinazolin-5-one as yellowish brown prisms, having a melting point of 96°-98°C (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03980645
Source datasetuspto-grants-1976_09
ORD IDord-04663eb65519407ab9db34a518a9f717
Source noteuspto-grants-1976_09