HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(1-Azetidinyl)butanal dimethylacetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-1,1-dimethoxybutane | HCID 122536 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(1-Azetidinyl)butanal dimethylacetal | HCID 23374585 | — |
Reaction Steps
A mixture of azetidine (2.0 g, 35.0 mmol), 4-chlorobutanal dimethylacetal (5.88 g, 39.0 mmol) and K2CO3 (5.38 g, 39.0 mmol), in anhydrous DMF (100ml), was stirred at room temperature for 72 h. Water (50 ml) was added and the mixture extracted with EtOAc (3×150 ml). The combined extracts were washed with H2O (3×50ml), dried (Na2SO4) and evaporated. The crude product was purified by distillation (1.2 g). δ (360 MHz, CDCl3) 1.35-1.42 (2H, m, CH2), 1.57-1.64 (2H, m, CH2), 2.00-2.40 (2H, m, CH2), 2.36 (2H, t, J=9.0 Hz, CH2), 3.15 (4H, m, t, J=7.0 Hz, 2 of CH2), 3.33 (6H, s, 2 of OMe), 4.35 (1H, t, J=5.7 Hz, CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567726 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-236248cb2e9f49cf85e4a869a7b084f4 |
| Source note | uspto-grants-1996_10 |