HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 178521301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178521301 | HCID 178521301 | 88.1% |
Reaction Steps
To a solution of ethanolamine (1.23 g, 20.1 mmol) in anhydrous MeOH (50 mL) at 0° C. was added benzaldehyde (2.13 g, 20.0 mmol) and molecular sieves (10 pieces). The resulting mixture was gradually warmed to room temperature and stirred for 120 h. The reaction mixture was filtered while rinsing with CH2Cl2. The filtrate was evaporated, and the residue was dried under vacuum overnight to afford off-white oily Compound 1 (2.63 g, 87%). The compound was used for the next step without further purification. 1H NMR (CDCl3) δ 2.40 (s, 1H), 3.70 to 3.80 (m, 2H), 3.85 to 4.0 (m, 2H), 7.35 to 7.50 (m, 3H), 7.68 to 7.79 (m, 2H), 8.32 (s, 1H); 8.11 (d, 2H); 13C NMR (CDCl3) δ 62.28, 63.17, 128.1, 128.52, 130.78, 135.72, 163.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115094B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-986b9e86dd2e4c86b71ba985e864a91a |
| Source note | uspto-grants-2015_08 |