Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-butyl N-methyl-N-(3-oxopropyl)carbamate | HCID 10442454 | — |
| Reactant | HCID 178418265 | HCID 178418265 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86587542 | HCID 86587542 | 65% |
Reaction Steps
Methyl-(3-oxopropyl)carbamic acid, 1,1-dimethylethyl ester (2.00 g, 10.7 mmol) was dissolved in tetrahydrofuran (20 ml) under nitrogen and cooled to 0° C. with stirring. To the resulting solution was added n-butylmagnesium chloride and the mixture stirred at 0° C. for a further 30 minutes and then allowed to warm to room temperature with stirring over 20 h. The mixture was then poured into saturated ammonium chloride solution and then extracted with diethyl ether three times. The combined organic fractions were then washed with brine and dried over magnesium sulfate. The solvent was evaporated and the residue eluted down a flash chromatography column using 40% diethyl ether/isohexane as eluent to give 1.70 g (65%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900243B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-4ceaf21c7df3403c91abc1cea555d38d |
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| Source note | uspto-grants-2005_05 |
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