HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277155Generated: October 30, 2026
Ammonium Acetate → 3-Amino-5-phenylthiopyran
https://huagongshe.com/reaction/277155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 12521138 | HCID 12521138 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Amino-5-phenylthiopyran | HCID 69596334 | 20.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355660B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-f9fd1191a52848599be1ea4aa9199410 |
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| Source note | uspto-grants-2002_03 |
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