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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276366Generated: October 28, 2026

Cyanogen Bromide → HCID 59323748, compound

https://huagongshe.com/reaction/2276366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium AcetateHCID 517045—
ReactantHCID 55282880HCID 55282880—
SolventMethanolHCID 887—
ProductHCID 59323748HCID 5932374841%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred, cooled (0° C.) solution of (RS)-2-amino-2-(3-fluoro-2-methyl-phenyl)-ethanol (1.82 g) and sodium acetate (1.72 g) in methanol (17 ml) was added dropwise a solution of cyanogen bromide (1.18 g) in methanol (8 ml) over 10 min. The mixture was then stirred for 1 h at 0° C., then was allowed to warm to at r.t. and stirring continued for 2 h. The mixture was concentrated in vacuo and the residue was resuspended in water and made basic by addition of 1 M aq sodium hydroxide solution. The mixture was then extracted twice with dichloromethane and the combined organic phases were dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (SiO2; gradient: dichloromethane/methanol) to give (RS)-4-(3-fluoro-2-methyl-phenyl)-4,5-dihydro-oxazol-2-ylamine (0.85 g, 41%) as a light yellow solid. MS (ISP): 195.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132136B2
Source datasetuspto-grants-2015_09
ORD IDord-67df041fb7244e8d98b9858273bfcc1a
Source noteuspto-grants-2015_09