HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52272Generated: October 28, 2026
Acetic Acid → (R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran
https://huagongshe.com/reaction/52272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 53650127 | HCID 53650127 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran | HCID 22871218 | 80.6% |
Reaction Steps
(R)-3-(N-Cyclobutylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran (1.01 g, 4.02 mmol) was dissolved in anhydrous methanol (20 mL) and to this was n-propionaldehyde (3.0 mL, 40.2 mmol) added. After 1 h the reaction was cooled (ice-bath) then sodium cyanoborohydride (0.46 g, 7.24 mmol) was added, the pH was adjusted to 4-5 with acetic acid and the reaction was allowed to stir at room temperature over the weekend. The solvent was removed in vacuo, the remains extracted thrice with diethyl ether. The combined ether portions were dried (MgSO4) filtered, and the solvent were taken into a 2M solution of NH3 and then removed in vacuo to give the crude residue. Chromatography on silica (eluent: 11% ethyl acetate/hexane) gave 0.95 g (80% yield) of the title compound as a clear oil. [α]21D =-95.4° (C=0.1; CHCl3) GC-MS (70 eV) M=293 (1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616610 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-52880a17bb9b4f3d90dd1edb0f188ee1 |
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| Source note | uspto-grants-1997_04 |
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