Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 69746561 | HCID 69746561 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 59067291 | HCID 59067291 | — |
Reaction Steps
To a cooled (0-5° C.) solution of (1S,2R,3S)-[l-(3,5-Difluoro-benzyl)-2,3-dihydroxy-heptyl]-carbamic acid tert-butyl ester (1.19 g, 3.2 mmol) in dioxane (20 mL) was added HCl (4 M in dioxane, 80 mL, 320 mmol) over 30 min. The reaction mixture was stirred at 0-5° C. for 30 min, then room temperature overnight. The volatiles were removed in vacuo and the residue was evaporated from ether to afford (1S,2R,3S)-1-(3,5-difluorobenzyl)-2,3-dihydroxyheptylamine as an HCl salt. MS (ESI+) for C14H21F2NO2 m/z 274.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06906104B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-7b3f9225dee24d5f9ae036d27f6a8b8f |
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| Source note | uspto-grants-2005_06 |
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