Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzyl 4-Hydroxy-1-piperidinecarboxylate | HCID 2794620 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19996229 | HCID 19996229 | — |
Reaction Steps
1-Benzyloxycarbonyl-4-hydroxypiperidine (15 g., 0.0638 mole) and N,N-diisopropylethylamine (12.3 ml., 9.13 g., 0.0707 mole) were dissolved in toluene (150 ml.), and the solution was added over 30 min. to a solution. of phosgene (12.63 g., 0.128 mole) in toluene (150 ml.). The reaction mixture was protected from. atmospheric moisture (drying tube), stirred magnetically, and kept at ambient temperature in a water bath during the addition. When the addition was complete the mixture was filtered and the solid residue washed with toluene (ca. 50 ml.). The solvent in the combined filtrate and washings was evaporated in vacuo (1 mm. pressure, solid CO2 cold finger condenser) to give 1-benzyloxycarbonyl-4-chlorocarbonyloxypiperidine, I.R. λ max 1775cm.-1 and 1700 cm.-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05039710 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-819ccbc19c5948e7ba6c697d67f02fcb |
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| Source note | uspto-grants-1991_08 |
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