Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chlormethyl-8-(1,1-dimethylethyl)-1,4-dioxaspiro(4.5)decan | HCID 14326294 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14326303 | HCID 14326303 | 98% |
Reaction Steps
6.5 g (0.0250 mol) of 8-t-butyl-2-chloromethyl-1,4-dioxaspiro[4.5]decane and 4.5 g (0.0450 mol) of cyclohexylamine are dissolved in 50 ml of 95% ethanol in the presence of 5.65 g (0.040 mol) of K2CO3 and 0.42 g (0.0025 mol) of KI in an autoclave. The mixture is heated to 180° C. for 8 hours with stirring. After returning to room temperature, the reaction medium is poured into 500 ml of water and extracted with 200 ml of CH2Cl2. The organic phase is dried over magnesium sulphate and concentrated under vacuum. The brown oil is used directly in the following step (yield: 98%; NMR analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856514 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-b21435b03ec6402ba7cefd062aaf17b6 |
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| Source note | uspto-grants-1999_01 |
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