Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 89838245 | HCID 89838245 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 89838555 | HCID 89838555 | — |
Reaction Steps
To 3.5 g of N-(tert-butyloxycarbonyl)-N′-(3-tert-butyl-4-methoxy-benzyl)piperazine 30 ml of 10% HCl and 5 ml of ethanol are added, the mixture is stirred for 5 h at 20° C., and evaporated to dryness in vacuum at 50÷80° C. Then 20 ml of dry acetone is added to the residue, the mixture is boiled with stifling for 20 min, then cooled down to 10° C. After 1 h the product is filtered off, washed with 10 ml of acetone and dried at the air. Yield of (3-tert-butyl-4-methoxybenzyl)piperazine dihydrochloride—2.2 g (68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249115B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-67368a519c574fa89754209ca64bfb62 |
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| Source note | uspto-grants-2016_02 |
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