Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethyl phosphoric acid | HCID 5166299 | — |
| Reactant | N-Benzyl-3-chloropropan-1-amine--hydrogen chloride (1/1) | HCID 20570562 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86704394 | HCID 86704394 | 63% |
Reaction Steps
1.6 mL of 37% aqueous formaldehyde solution is added to a suspension of N-benzyl-3-chloropropan-1-amine hydrochloride (7.9 g or 35.9 mmol) in dioxane (60 mL), the resulting mixture is slightly heated until it becomes a solution. The solution is cooled to room temperature, 3.2 mL of diethyl phosphate is added thereto, stirring at room temperature for 30 min, and then stirring at 90-100° C. for 3 h, the reaction is completed. The solvent is removed under reduced pressure, and the residue is purified by column chromatography (eluent: 1-4% MeOH in DCM) to obtain 7.6 g target compound (yield: 63%). The analytical data of the obtained product are as follows: 1HNMR (400 MHz, DMSO-d6): δ=7.30-7.21 (m, 5H), 4.01-3.93 (m, 4H), 3.69 (s, 2H), 3.59 (t, J=6.8 Hz, 2H), 2.83 (d, J=10.0 Hz, 2H), 2.61 (t, J=6.8 Hz, 2H), 1.85-1.82 (m, 2H), 1.2 (t, J=7.2 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933230B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-dadddb24e7624a369ac20a3c2c33ff24 |
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| Source note | uspto-grants-2015_01 |
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