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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49440Generated: October 29, 2026

Ammonium Acetate → 3-Amino-5-phenylthiopyran

https://huagongshe.com/reaction/49440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 12521138HCID 12521138—
SolventMethanolHCID 887—
Product3-Amino-5-phenylthiopyranHCID 6959633420.1%

Reaction Steps

This compound was prepared as shown in Scheme 25. Thus, to 0.96 g (5 mmol) of 5-phenyl-3-thiopyranone (P. T. Lansbury, et al., J. Am. Chem. Soc. 1970, 92, 5649) in 50 mL of anhydrous methanol was added 7.7 g (100 mmol) of ammonium acetate and 6.5 g of 3A molecular sieves. After stirring 30 minutes at room temperature, 1.25 g (20 mmol) of sodium cyanoborohydride was added portionwise. After stirring 16 hours, the mixture was gravity filtered, and the methanol was evaporated under vacuum. The residue was partitioned between ice/HCl and ether. The acidic aqueous phase was extracted twice more with ether, then it was made basic with ice and 50% NaOH aqueous. The mixture was extracted with CH2Cl2, dried (MgSO4), and evaporated to give 0.19 g (20%) of the title compound. GC/MS showed 100% purity with a molecular ion of 193.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706740B2
Source datasetuspto-grants-2004_03
ORD IDord-465cbec955d34fad9ff70c0b08ba40cc
Source noteuspto-grants-2004_03