HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051928Generated: November 2, 2026
Acetone Cyanohydrin → HCID 90303212, compound
https://huagongshe.com/reaction/1051928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | HCID 90303245 | HCID 90303245 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90303212 | HCID 90303212 | — |
Reaction Steps
To a mixture of 6,7-dihydro-5H-pyrano[2,3-d]thiazol-7-ol (0.65 g, 4.14 mmol), acetone cyanohydrin (880 mg, 10.3 mmol) and (n-Bu)3P (1.67 g, 8.27 mmol) in THF (79 mL) was added at 0° C. 1,1′-(azodicarbonyl)dipiperidine (2.09 g, 8.27 mmol). The mixture was stirred at 0° C. for 30 min, then, it was allowed to warm to RT and was stirred for 2 h. Subsequently, the reaction mixture was diluted with diisopropyl ether, filtrated and the filtrate was conc. in vacuo. Purification by means of CC (5-70% EtOAc/Hept) provided a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388197B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-2db5a96026d5415e9c1cc21caca724ad |
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| Source note | uspto-grants-2016_07 |
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