HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylamine, (-)- → ((1S)-1-Phenylethyl)(1,4-dioxaspiro[4.5]dec-8-yl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | ((1S)-1-Phenylethyl)(1,4-dioxaspiro[4.5]dec-8-yl)amine | HCID 5712106 | 67% |
Reaction Steps
1,4-Dioxaspiro[4.5]decan-8-one (10 g, 64.03 mmol) was dissolved in dry dichloroethane (300 mL) under an atmosphere of nitrogen. (1S)-1-phenylethylamine (8.96 mL, 70.43 mmol) was added neat at room temperature followed by sodium triacetoxyborohydride (20.36 g, 96.04 mmol) neat in small portions. The reaction was stirred at room temperature overnight. The reaction was quenched by the addition of distilled water (200 mL). The phases were separated and the aqueous phase was extracted with dichloromethane. The combined organic phases were dried over sodium sulfate. The filtrate was concentrated under reduced pressure. A yellow oil was obtained of satisfactory purity based on (11.2 g, 67% yield). M+1: 262.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723340B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-c4d886398ab3438f9e68d0b3c3922404 |
| Source note | uspto-grants-2010_05 |