Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Decyl glycidyl ether | HCID 92960 | — |
| Reactant | Ammonium Carbamate | HCID 517232 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131716215 | HCID 131716215 | — |
Reaction Steps
The ammonium carbamate prepared as described above was dissolved in anhydrous methanol (a total of 3.5 L) and transferred to a five liter three-necked round bottom flask equipped with thermometer and magnetic stirrer. (Decyloxy)methyloxirane (150 g, 0.7 mole) was added and the mixture was stirred at ambient temperature for five days, after which no more epoxide could be detected by TLC (silica gel, 4:1 hexane:methyl t-butyl ether, Rf =0.62). A small amount of precipitate was observed. The mixture was cooled to 5° C. and suction filtered on a coarse frit. After drying, 8.2 g of white solid was obtained. The methanol solution was evaporated to dryness on a rotary evaporator at about 5 mm Hg and a bath temperature of about 40° C. The crude substituted ammonium carbamate was obtained as a white solid (161 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04931596 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-1274ca8c9fd74f909e202be20fa3f308 |
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| Source note | uspto-grants-1990_06 |
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