HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-[(Tert-butyldimethylsilyl)oxy]-2-chlorobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-Chloro-4-hydroxybenzaldehyde | HCID 185363 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[(Tert-butyldimethylsilyl)oxy]-2-chlorobenzaldehyde | HCID 58907469 | 75% |
Reaction Steps
A solution of 2-chloro-4-hydroxybenzaldehyde (5.0 g, 32 mmol), tert-butyl(dimethyl)silyl chloride (5.3 g, 35 mmol), imidazole (2.9 g, 45 mmol) and N,N-dimethylaminopyridine (10 mg) in N,N-dimethylformamide (40 ml) was stirred at room temperature under a nitrogen atmosphere for 16 hours. The solvent was removed in vacuo and the residue partitioned between ethyl acteate (100 ml) and water (100 ml). The organic phase was separated, washed with sat. aq. sodium chloride (50 ml), dried (sodium sulfate) and reduced in vacuo. Further purification by column chromatography on silica gel eluting with pentane:ethyl acetate (3:1 changing to 2:1) gave the title compound as a colourless oil (6.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244766B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-fd507c1fbf134d1293ebfd7e050cb1be |
| Source note | uspto-grants-2007_07 |