HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Isopropyl-1,3-thiazole-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ethyl 4-isopropylthiazole-2-carboxylate | HCID 10821861 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Isopropyl-1,3-thiazole-2-carbaldehyde | HCID 11084110 | — |
Reaction Steps
A solution of 2.1 g (11 mmol) of 4-isopropyl-thiazole-2-carboxylic acid ethyl ester (J. Med. Chem., 1998:602-617) in CH2Cl2 (50 mL) was cooled to −78° C. under nitrogen and treated dropwise with DIBAL (12 mL of 1.0 M in CH2Cl2; 12 mmol). The mixture was stirred at low temperature for 1 hour and then treated with another 7 mL of DIBAL. The solution was stirred for 30 minutes at −78° C. H2O was added, and the mixture was extracted with EtOAc (3×100 mL). The combined extracts were washed with brine, dried (MgSO4), and concentrated. Chromatography of the residue over silica gel, eluting with 3:1 hexane:EtOAc, gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528510B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-66f7959fcba9427bb81462d27ea3cefe |
| Source note | uspto-grants-2003_03 |