Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | HCID 10607353 | HCID 10607353 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10487130 | HCID 10487130 | 70.7% |
Reaction Steps
A suspension of 9.6 g (0.054 moles) of 3-chloro-5,5-dimethyl-2-oxoperhydroazepine and 18.98 g (0.054 moles) of Ba(OH)2.8H2O in 250 ml of water, was heated in a Parr apparatus at 110° C. for 2 hours. Then, 7.22 g (0.054 moles) of ammonium sulphate were added. The precipitate was filtered off, and the solution was evaporated in vacuo to dryness. The residue was treated with hot 2-propanol and filtered to afford a white solid which was dissolved in water and passed over an ion-exchange column (Dovex 50). The residual salts were removed with 200 ml of water and the aminoacid was eluted with 2N ammonium hydroxide to yield 6.0 g of 4,4-dimethyl pipecolic acid. M.P. >300° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05089507 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-3138f1d3cffd4271bfa6d8d48be0343f |
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| Source note | uspto-grants-1992_02 |
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