Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl squarate | HCID 123228 | — |
| Reactant | Carbamic acid, [3-[(cyanomethyl)amino]propyl]-, 1,1-dimethylethyl ester | HCID 10560546 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10806855 | HCID 10806855 | 90.2% |
Reaction Steps
A solution of 3,4-diethoxy-3-cyclobutene-1,2-dione (2.6 mL, 18 mmol) in absolute ethanol (90 mL) was treated with [3-(cyanomethylamino)propyl]carbamic acid 1,1-dimethylethyl ester (3.90 g, 18 mmol) in ethanol (30 mL) over 90 min. After 40 hours the reaction mixture was evaporated, dissolved in dichloromethane, preadsorbed onto silica gel, and purified by flash chromatography (7 cm diameter, gradient elution with 0-5% methanol in dichloromethane) to yield [3-[(cyanomethyl)-(2-ethoxy-3,4-dioxo-1-cyclobuten-1-yl)amino]propyl]carbamic acid 1,1-dimethylethyl ester as a yellow oil (5.48 g, 90%); IR (neat, cm-1): 3360, 1800; MS (+FAB): 282 (76), 238 (98), 158 (100); 1H NMR (CDCl3, 400 MHz): δ 4.81 (q, J=7 Hz, 2H), 4.75 (br s, NH), 4.45, 3.66 (s, 2H), 3.84, 3.60 (br m, 2H), 3.26-3.15 (m, 2H), 1.91 (p, J=6.5 Hz, 2H), 1.50 (t, J=7 Hz, 3H), 1.45 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240946 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-5743054727df44bfab2054b7ea21e3dc |
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| Source note | uspto-grants-1993_08 |
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