HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 57270951, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 2,5-Bis(3-methoxy-2,4,6-trinitrophenyl)-1,3,4-oxadiazole | HCID 12377582 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57270951 | HCID 57270951 | — |
Reaction Steps
A solution of 0.3 g (0.0049 mole) of ethanolamine in 20 ml of methanol was stirred in an ice bath during the addition of 1.0 g (0.0018 mole) of 2,5-bis(3-methoxy-2,4,6-trinitrophenyl)-1,3,4-oxadiazole. After 10 min. at 0° C., the mixture was stirred at room temperature for 5 hr. before the crude product [1.1 9 (94%), mp 250° dec] was removed by filtration. Digestion with boiling acetone gave the purified product, as an insoluble yellow solid, mp 264° C. dec.; 1H NMR (DMSO-d6 +D2O): 3.22 (t, 4H), 3.70 (t, 4H), 9.32 (s, 2H); IR(KBr): 3700-3200 (OH and NH), 1610, 1625 (C=N), 1545, 1340 (NO2). Anal. Calcd. for C18H14N10O15 : C, 35.42; H, 2.31; N, 22.95. Found: C, 35.62; H, 2.30; N, 22.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081255 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-ecf415608b1a4d69aa9d9adb2f68df18 |
| Source note | uspto-grants-1992_01 |