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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421606Generated: October 31, 2026

1-Phenethylamine, (-)- → ((1S)-1-Phenylethyl)(1,4-dioxaspiro[4.5]dec-8-yl)amine

https://huagongshe.com/reaction/421606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
Product((1S)-1-Phenylethyl)(1,4-dioxaspiro[4.5]dec-8-yl)amineHCID 571210667%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101588B2
Source datasetuspto-grants-2012_01
ORD IDord-becd6dd5f7f040bb89da1ff059685595
Source noteuspto-grants-2012_01