HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56433Generated: October 29, 2026
1-Phenethylamine, (+)- → HCID 118036275, compound
https://huagongshe.com/reaction/56433
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | 4,4-Dimethyl-3,7-dioxa-bicyclo[4.1.0]heptane | HCID 118036227 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 118036275 | HCID 118036275 | — |
| Product | (4S,5S)-2,2-dimethyl-5-((R)-1-phenylethylamino)-tetrahydro-2H-pyran-4-ol | HCID 118036302 | — |
Reaction Steps
A mixture of 4,4-dimethyl-3,7-dioxa-bicyclo[4.1.0]heptane (7.0 g, 54 mmol) and (R)-1-phenylethanamine (9.9 g, 82 mmol) in isopropanol (50 mL) was stirred at 80° C. for 6 days. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography (elute:petroleum ether:dichloromethane containing 1% ammonia-methanol (7 M), 10:1 to dichloromethane containing 1% ammonia/methanol (7 M) to afford (4R,5R)-2,2-dimethyl-5-((R)-1-phenylethylamino)-tetrahydro-2H-pyran-4-ol (6a) (more polar fraction, 1.5 g) and (4S,5S)-2,2-dimethyl-5-((R)-1-phenylethylamino)-tetrahydro-2H-pyran-4-ol (6b) (less polar fraction, 1.7 g) as a yellow oil. Note: The absolute configuration of the products was assigned randomly. MS (ES+) C15H23NO2 requires: 249, found: 250 [M+H]+. Mobile phase for TLC: ethyl acetate/dichloromethane=2/1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434700B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-5912bb3598984fe99e50495da4685d2d |
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| Source note | uspto-grants-2016_09 |
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