Carbon Dioxide → HCID 15187618, compound
Reaction equation
Cl.C(ON)C.C(N(CC)CC)C.C(=O)=O.C[Si](C)(C)Cl.[CH3:21][Si:22]([O:25][C:26](=[O:35])[N:27]([O:32][CH2:33][CH3:34])[Si](C)(C)C)([CH3:24])[CH3:23]>C(OCC)C>[CH3:24][Si:22]([O:25][C:26](=[O:35])[NH:27][O:32][CH2:33][CH3:34])([CH3:21])[CH3:23]Participants
Procedure
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.
Sources & evidence
- ORD record
- ord-69e8dda3d044442fb97e0187bab26a47
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04831173
Reaction notes
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