HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-(1-Fluorocyclobutyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Cyclopropylbenzaldehyde | HCID 11506474 | — |
| Reactant | 1-Bromo-4-(1-fluorocyclobutyl)benzene | HCID 68564159 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-(1-Fluorocyclobutyl)benzaldehyde | HCID 84718020 | — |
Reaction Steps
The title compound was synthesized in analogy to 4-cyclopropyl benzaldehyde (described in example S1-A) using 1.64 g of 1-bromo-4-(1-fluoro-cyclobutyl)-benzene (7.16 mmol), 4.92 ml of a 1.6 molar solution of n-BuLi in hexane (7.87 mmol) and 1.1 ml of DMF (14.32 mmol). 4-(1-Fluoro-cyclobutyl)-benzaldehyde was isolated as crude product as a light yellow liquid (1.23 g, 96%). 1H NMR (CDCl3, 300 MHz): δ 1.84 (m, 1H), 2.15 (m, 1H), 2.49-2.81 (m, 5H), 7.63 (d, J=8 Hz, 2H), 7.92 (d, J=8 Hz, 2H), 10.03 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745477B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bb6f4adb33084144b99c3ec8cb6c4e5d |
| Source note | uspto-grants-2010_06 |