HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007521Generated: October 28, 2026
3-Phenylpropylamine → HCID 178518606, compound
https://huagongshe.com/reaction/1007521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenylpropylamine | HCID 16259 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(4-oxocyclohexyl)-1,3-benzoxazol-2(3H)-one | HCID 9813382 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178518606 | HCID 178518606 | 42.8% |
Reaction Steps
To a solution of ketone 5 (0.50 g, 2.0 mmol) in 2-propanol (30 mL) was added 3 Å molecular sieves and 3-phenyl-1-propylamine 10 (0.39 g, 2.0 mmol). The reaction mixture was stirred for 4 hours. Sodium borohydride (0.11 g, 2.83 mmol) was added, and the reaction mixture was stirred overnight, quenched with MeOH, and concentrated under reduced pressure. Purification by flash chromatography (silica, 9.5:5:1 CH2Cl2:MeOH:NH4OH) gave 6-[trans-4-(3-phenylpropylamino)-cyclohexyl]-3H-benzoxazol-2-one (0.30 g, 42%): mp 166-170° C.; IR (KBr): 2933, 1761, 1653, 1582 cm−1; 1H NMR (500 MHz, DMSO-d6): δ 9.09 (s, 1H), 7.30-7.19 (m, 6H), 7.03 (d, J=9 Hz, 1H), 6.68 (d, J=9 Hz, 1H), 2.66 (m, 1H), 2.55 (t, J=8 Hz, 2H), 2.37 (tt, J=10, 2 Hz, 1H), 1.98 (d, J=10 Hz, 1H), 1.96 (d, J=10 Hz, 1H), 1.76 (d, J=3 Hz, 1H), 1.56 (m, 1H), 1.45 (m, 1H), 1.39 (m, 1H), 1.18-1.05 (m, 6H); CI-MS (methane) (m/z): 351 [M+H]+; HRMS-API (m/z): [M+H]+ calcd for C22H26N2O2, 351.2072; found, 351.2178; HPLC: method A, 7.66 minutes (96.9%); method B, 14.14 minutes (97.7%); Anal. Calcd for C22H26N2O2.H2O: C, 71.71; H, 7.66; N, 7.60. Found: C, 71.70; H, 7.62; N, 7.20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794402B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-875bfb8b957c4d798ca6d1d469b1f547 |
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| Source note | uspto-grants-2004_09 |
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