HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Isopropylthiazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 5-isopropylthiazole-4-carboxylate | HCID 13015587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Isopropylthiazole-4-carbaldehyde | HCID 11137386 | — |
Reaction Steps
A solution of 6.8 g (37 mmol) of 5-isopropyl-thiazole-4-carboxylic acid methyl ester (J. Chem. Soc., Perkin Trans. 1, 1982:159-164) in CH2Cl2 (120 mL) was cooled to −78° C. under nitrogen and treated dropwise with DIBAL (37 mL of 1.0 M in CH2Cl2; 37 mmol). The mixture was stirred at low temperature for 45 minutes and then treated with another 20 mL of DIBAL. The solution was stirred for 1 hour at −78° C. H2O was added, and the mixture was extracted with EtOAc (3×150 mL). The combined extracts were washed with brine, dried (MgSO4), and concentrated. Chromatography of the residue over silica gel, eluting with 2:1 hexane:EtOAc, gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852711B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-530d04ee3212479b9a176b43e26151ce |
| Source note | uspto-grants-2005_02 |