HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → 2-Thiophenecarboxaldehyde, 4,5-dichloro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Thiophene, 2,3-dichloro- | HCID 140207 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Thiophenecarboxaldehyde, 4,5-dichloro- | HCID 149424 | — |
Reaction Steps
11.1 g of diisopropylamine in 100 ml of tetrahydrofuran were cooled to -60° C., 49 ml of n-butyllithium were added over 10 minutes. The mixture was stirred for 30 minutes and 10 g of 2,3-dichlorothiophene were added at -60° C. The mixture was stirred for 45 minutes and then 6 m1 of dimethylformamide and 10 ml of tetrahydrofuran were added. The mixture was stirred for 1 and a half hours, allowed to return to room temperature, poured into a saturated aqueous sodium dihydrogenphosphate solution and extracted with isopropyl ether. The solvent was evaporated and, after chromatography on silica (eluent: 95/5 hexane/ethyl acetate), 10.16 g of the expected product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405865 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-2e9d3e95778b41dd87a9ba5027be5b93 |
| Source note | uspto-grants-1995_04 |