HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → Tert-butyl 2-{[(benzyloxy)carbonyl]amino}-2-cyanoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-{[(Benzyloxy)carbonyl]amino}-2-cyanoacetic acid | HCID 18942734 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 2-{[(benzyloxy)carbonyl]amino}-2-cyanoacetate | HCID 18942739 | 67.4% |
Reaction Steps
To a mixture of 2-benzyloxycarbonylamino-2-cyanoacetic acid (2.00 g, 8.54 mmol), toluene (20 ml) and t-butyl alcohol (6.33 g, 85.4 mmol), was added trifluoroacetic acid anhydride (7.17 g, 34.2 mmol) dropwise and the solution was stirred for half an hour. The reaction solution was neutralized by adding 10% NaOH aqueous solution (18 g), the organic layer was separated and washed with water three times, dried over sodium sulfate, insoluble materials were filtered and the filtrate was condensed to give t-butyl 2-benzyloxycarbonylamino-2-cyanoacetate (1.67 g, yield 67.4%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030486B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-1ca1ccfb4fae4a2b8134c3bf67a5e4c5 |
| Source note | uspto-grants-2011_10 |