HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75178Generated: October 28, 2026
Potassium Carbonate → (3-Cyano-3-butene-1-yl)(ethoxycarbonyl)azanyl 1,1-dimethylethyl carbonate
https://huagongshe.com/reaction/75178
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylsulfonyloxy-2-(hydroxymethyl) butanenitrile | HCID 86674470 | — |
| Reactant | 1,1-Dimethylethyl (ethoxycarbonyl)azanyl carbonate | HCID 86674471 | — |
| Reactant | 1,1-Dimethylethyl(ethoxycarbonyl)azanyl carbonate | HCID 86674472 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3-Cyano-3-butene-1-yl)(ethoxycarbonyl)azanyl 1,1-dimethylethyl carbonate | HCID 86674469 | — |
Reaction Steps
A mixture of 4-methylsulfonyloxy-2-(hydroxymethyl) butanenitrile (i.e. the product of Step E) (6.87 g, 0.039 mol), 1,1-dimethylethyl (ethoxycarbonyl)azanyl carbonate (7.65 g, 0.037 mol) (i.e. the product of Step F) and potassium carbonate (10.21 g, 0.074 mol) in N,N-dimethylformamide (50 mL) was stirred at room temperature for 20 h. The reaction mixture was poured onto iced water (100 mL) and extracted with diethyl ether (3×50 mL). The combined organic layers were washed with water (50 mL) and concentrated to a pale-tan oil (10.05 g). The oil was adsorbed onto Celite® (diatomaceous filter aid), and then purified by silica gel chromatography (0-100% gradient of ethyl acetate in petroleum ether as eluant). The appropriate fractions were combined to provide the title compound as a yellow oil (3.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835427B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b33f2e5e72ee4041adbf8b4167d0f42f |
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| Source note | uspto-grants-2014_09 |
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