HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-(4-Fluorophenyl)pyridine-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-(4-Fluorophenyl)pyridine-3-carboxylic acid morpholinamide | HCID 69529009 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-Fluorophenyl)pyridine-3-carbaldehyde | HCID 9877671 | 98% |
Reaction Steps
6.0 g of 5-(4-fluorophenyl)pyridine-3-carboxylic acid morpholinamide from Example 1(b) are dissolved in 30 ml of THF, and 57 g of a 13.6% LiAlH—(OEt)3 solution in THF are added over the course of 10 minutes at 30° C. to 35° C. After 1 hour, 30 ml of 12.5% sulfuric acid are added, and the organic phase is separated off. The aqueous phase is adjusted to pH 1 using sulfuric acid and extracted a number of times with methyl tert-butyl ether. The organic phases are then combined, extracted once with water and then evaporated, leaving a residue of 4.3 g having a content of 97% by weight of 5-(4-fluorophenyl)pyridine-3-carbaldehyde (yield=98% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528256B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-a699c572706340d2b27d7bc42d0668d1 |
| Source note | uspto-grants-2009_05 |