Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 2757206 | HCID 2757206 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18322378 | HCID 18322378 | 66% |
Reaction Steps
To a solution of 3-(N-carbo-tert-butoxyamino)-5-tert-butylthiophene-2-carboxylic acid (0.20 g, 0.67 mmol), allyl alcohol (0.042 g, 0.73 mmol, 1.1 equiv) and DMAP (0.008 g, 0.07 mmol, 10 mol %) in CH2Cl2 (2 mL) was added EDCI.HCl (0.14 g, 0.73 mmol, 1.1 equiv). The CH2Cl2 mixture was stirred at room temp. for 3 d, diluted with CH2Cl2, washed with a 1N HCl solution (5 mL) and a saturated NaHCO3 solution (5 mL), dried (Na2SO4), and concentrated under reduced pressure to afford allyl 3-(N-carbo-tert-butoxyamino)-5-tert-butylthiophene-2-carboxylate (0.15 g, 65%) as a colorless oil: TLC (50% CH2Cl2/hexane) Rf0.63; 1H NMR (CDCl3) δ1.37 (s, 9H), 1.50 (s, 9H), 4.74 (ddd, J=5.5, 1.5, 1.5 Hz, 2H), 5.26 (dd, J=10.3, 1.5 Hz, 1H), 5.37 (dd, J=17.3, 1.5 Hz, 1H), 5.87-5.98 (m, 1H), 7.68, 9.35; 13C NMR (CDCl3) δ28.2 (3C), 31.8 (3C), 35.2, 64.9, 80.8, 104.9, 116.4, 118.1, 132.0, 145.6, 152.1, 164.0, 164.4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344476B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-2618625a33da4f3597ff8398c83c008a |
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| Source note | uspto-grants-2002_02 |
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