HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 59707722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | (Dimethylamino)ethyl methacrylate | HCID 17869 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59707722 | HCID 59707722 | — |
Reaction Steps
5 g 2-(Dimethylamino)ethyl methacrylate and 8.68 g tert-butyl bromoacetate were reacted in 20 ml acetonitrile for 24 h at 50° C. under N2 protection. Upon addition of 250 ml ethyl ether to the reaction mixture, the formed white crystals were isolated and dried. The resulting CB-tBu monomers were immediately stored in a desiccator at −20° C. (yield 96%). 1H NMR (D2O) δ (ppm): 1.44 (s, 9H, —OC(CH3)3), 1.87 (s, 3H, CH2═C(CH3)COO—), 3.31 (s, 6H, —CH2N(CH3)2CH2COO—), 3.98 (t, J=3 Hz, 2H, CH2═C(CH3)COOCH2CH2N(CH3)2CH2—), 4.28 (s, 2H, —CH2N(CH3)2CH2COO—), 4.60 (t, J=3 Hz, 2H, CH2═C(CH3)COOCH2CH2N(CH3)2CH2—), 5.73 and 6.10 (s, 2H, CH2═C(CH3)COO—).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08617592B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-edd6911c9ee940838b238d518e6daa47 |
| Source note | uspto-grants-2013_12 |