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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223009Generated: October 30, 2026

Ammonia → HCID 11245365, compound

https://huagongshe.com/reaction/2223009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrogen PeroxideHCID 784—
ReactantHCID 11210088HCID 11210088—
SolventEthanolHCID 702—
ProductHCID 11245365HCID 11245365—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

To a stirring solution of (S)-3-hydroxy-4-trityloxybutanenitrile (5.15 g, 15.01 mmol) in 15 mL of ethanol at room temperature was added aqueous NH3 (50 mL) and H2O2 (100 vol.) (34 mL, 300.00 mmol) was added in portions while maintaining the temperature of the reaction mixture below 25° C. After complete addition, the resultant reaction mixture was stirred vigorously at 25-30° C. and the reaction progress was monitored by TLC. On completion of the reaction (overnight) as indicated by the TLC, the reaction volume was concentrated to about 50% of the original volume under reduced pressure and the resultant mixture was extracted with dichloromethane (3×75 mL). The combined organic layers were dried over anhydrous Na2SO4 and the solvent was evaporated to leave a residue, which was purified by column chromatography employing EtOAc-hexane (80:20) as eluent to afford (S)-3-hydroxy-4-trityloxy butanamide in almost quantitative yield. m.p. 96-100° C.; [α]27D=−18.08 (c 1.0, MeOH); IR (KBr) 3467, 3349, 3012, 2980, 2918, 2839, 1671, 1098, 1076 cm−1; 1HNMR (300 MHz, CDCl3) δ 2.36 (d, 2H, J=6.5 Hz), 3.13-3.16 (m, 2H), 3.28 (6S, 1H), 4.11-4.15 (m, 1H), 5.44 (br, s, 1H), 7.18-7.38 (m, 9H), 7.39-7.42 (m, 6H); Mass (EI) 361, 259, 243, 165, 77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07374926B2
Source datasetuspto-grants-2008_05
ORD IDord-bf67b0b762c04ab28f743b8feb721a44
Source noteuspto-grants-2008_05