HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-(Tert-butyldimethylsilyloxymethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Tert-butyldimethylsilyloxymethyl)aniline | HCID 10585977 | 62.4% |
Reaction Steps
To 1.00 g (8.1 mmol) of 3-hydroxymethylaniline in 25 mL of DMF was added 0.61 g (8.9 mmol) of imidazole and 1.35 g (8.9 mmol) of tert-butyldimethylsilyl chloride. The reaction was stirred at room temperature for 18 h and poured into 12 volumes of water. The product was extracted with ether and the combined organic layers were washed successively with water and brine, dried over sodium sulfate, filtered and concentrated to a golden oil. The oil was purified by flash chromatography eluting with a 20% ethyl acetate/hexanes mixture to give 1.2 g (62%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714009B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-d60200cf16e44e9dba486b1f40d236c8 |
| Source note | uspto-grants-2010_05 |