HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825902Generated: October 30, 2026
2-Methoxyethylamine → HCID 67311514, compound
https://huagongshe.com/reaction/1825902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 2-Propenoic acid, 3-(4-formylphenyl)- | HCID 98077 | — |
| Reactant | Cinnamaldehyde | HCID 637511 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67311514 | HCID 67311514 | — |
Reaction Steps
Wang resin (1.1 mmol/g, 1.00 g) in a polypropylene filtration tube with a polyethylene frit was added DMF (5 mL) and CH2Cl2 (5 mL), followed by 4-formylcinnamic acid (5.5 mmol, 969 mg), DMAP (1.08 mmol, 132 mg) and diisopropylcarbodiimide (5.5 mmol, 861 μL). The mixture was shaken at room temperature for 24 hours. The resulting resin was washed with DMF (3×5 mL), MeOH (3×5 mL) and CH2Cl2 (4×5 mL), then dried in vacuo. To the resin (100 mg) was added 2-methoxyethylamine (1.1 mmol, 96 μL) in DMF (1 mL), Na(OAc)3BH (2.2 mmol, 466 mg) and acetic acid (25 μL). After shaking at room temperature overnight, the resulting resin was washed with DMF (3×1 mL), MeOH (3×1 mL) and CH2Cl2 (4×1 mL), then dried in vacuo. The resulting resin was suspended in a solution of trans-cinnamaldehyde (1.1 mmol, 139 μL), Na(OAc)3BH (2.2 mmol, 466 mg) and acetic acid (10 μL) in DMF (1 mL). The mixture was shaken at room temperature for 24 hours. The resulting resin was washed with DMF (3×1 mL), MeOH (3×1 mL) and CH2Cl2 (4×1 mL), then dried in vacuo. To the dry resin was added polyamine resin and CH2Cl2. The mixture was agitated at room temperature for 24 hours, then filtered and washed with CH2Cl2 (2×1.5 mL). The filtrates were collected and evaporated to yield 21 as a colorless oil (LRMS m/z 351).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07049329B2 |
|---|
| Source dataset | uspto-grants-2006_05 |
|---|
| ORD ID | ord-74db979cf12b466abe8160e52dec677a |
|---|
| Source note | uspto-grants-2006_05 |
|---|