Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | 4-Nitrobenzyl chloroformate | HCID 78205 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 3102539 | HCID 3102539 | — |
Reaction Steps
5 g (44.2 mmole) of ε-caprolactam was dissolved in 19.48 g of 20 wt % NaOH and heated to reflux for 3-5 hours. After ε-caprolactam was hydrolyzed completely, the mixture was cooled down to 5˜10° C. and then 25 g of water and 10 g of 4-nitrobenzyl chloroformate were added. The mixture was stirred 1 hour at 5-10° C. and then washed with 25 g of ethyl acetate twice. The pH of the aqueous layer was adjusted to 1-2 by adding 16% HCl and extracted with ethyl acetate twice. Combined ethyl acetate layer was washed with water. The organic layer was dried by sodium sulfate and concentrated to obtain 6-(4-nitro-benzyloxycarbonylamino)-hexanoic acid. Purity was 93.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809581B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-b540da79fe3140c79903bf867ce95f79 |
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| Source note | uspto-grants-2014_08 |
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