HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (S)-4-(tert-butyldimethylsilyloxy)butan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (+)-1,3-Butanediol | HCID 446973 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-4-(tert-butyldimethylsilyloxy)butan-2-ol | HCID 10998136 | — |
Reaction Steps
A 0° C. solution of (S)—(+)-1,3-butanediol (2.1 g, 23.3 mmol), imidazole (1.74 g, 25.6 mmol), and N,N-dimethylformamide (1.0 mL) in dichloromethane (40 mL) was treated with tert-butyl-dimethylsilyl chloride (3.68 g, 23.3 mmol). The reaction mixture was warmed to room temperature, stirred overnight, quenched with saturated aqueous ammonium chloride and extracted with dichloromethane. The combined dichloromethane layers were dried (MgSO4), filtered and concentrated to afford of the desired product of sufficient purity for subsequent use without further purification in near quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559140B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-52f880592c4b40639a7e41c83a8a1b86 |
| Source note | uspto-grants-2003_05 |