Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | HCID 15187619 | HCID 15187619 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15187618 | HCID 15187618 | — |
Reaction Steps
49 g (0.5 mole) of ethoxyamine hydrochloride and 151.5 g (1.5 mole) of triethylamine in 250 ml of dry diethyl ether is treated with carbon dioxide in the same apparatus and same conditions as described in Example 1a. After the carbon dioxide uptake has been finished, 108.5 g (1 mole) of trimethylchlorosilane is added to the reaction mixture over 1.5 hours under vigorous stirring. Following the same procedure as in Example 1a., a mixture of N-ethoxy,N-trimethylsilylcarbamic acid trimethylsilyl ester and N-ethoxycarbamic acid trimethylsilyl ester is obtained. Distillation under reduced pressure give 28.3 g (0.16 mole, 32%; b.p.: 42-45° C./2.5 mbar) of N-ethoxycarbamic acid trimethylsilyl ester and 72.1 g (0.29 mole, 58%; b.p.: 87-91° C./2.5 mbar) of N-ethoxy,N-trimethylsilylcarbamic acid trimethylsilyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04831173 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-69e8dda3d044442fb97e0187bab26a47 |
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| Source note | uspto-grants-1989_05 |
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