HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(13-tert-Butoxycarbonylamino-tricyclo[8.2.1.03,8]trideca-3(8),4,6-trien-5-yl)-acrylic acid methyl ester → 3-(13-tert-Butoxycarbonylamino-tricyclo-[8.2.1.03,8]trideca-3(8),4,6-trien-5-yl)-propionic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(13-tert-Butoxycarbonylamino-tricyclo[8.2.1.03,8]trideca-3(8),4,6-trien-5-yl)-acrylic acid methyl ester | HCID 69666271 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(13-tert-Butoxycarbonylamino-tricyclo-[8.2.1.03,8]trideca-3(8),4,6-trien-5-yl)-propionic acid methyl ester | HCID 69666459 | 94.3% |
Reaction Steps
3-(13-tert-Butoxycarbonylamino-tricyclo[8.2.1.03,8]trideca-3(8),4,6-trien-5-yl)-acrylic acid methyl ester (300 mg, 0.809 mmol, prepared in Example 32 Step 3) and 20% palladium hydroxide on carbon (30 mg) in ethanol (30 ml) were stirred under 1 atm. of hydrogen at room temperature for 18 hours. The mixture was filtered through Celite and the filtrate concentrated to give a colourless oil 285 mg (94%). 1H NMR (CDCl3, 400 MHz) δ 7.00 (1H, d, J=8.2 Hz), 6.90 (2H, m), 4.97 (1H, m), 4.03 (1H, m), 3.67 (3H, s), 2.99 (2H, m), 2.89 (2H, m), 2.55–2.62 (4H, m), 2.48 (2H, m), 1.71 (2H, m), 1.47 (9H, s), 1.19 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138400B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-c0cb8351b3b949cbbf8065547eeba788 |
| Source note | uspto-grants-2006_11 |