HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehyde → (1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehyde | HCID 13600235 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)methanol | HCID 21877600 | 89.6% |
Reaction Steps
A solution of 1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-imidazole-2-carboxaldehyde (prepared according to procedures described by J. P. Whitten et al., J. Org. Chem., 51 (1986), 1891) (9.95 g, 44.0 mmol) in dry ether (40 ml) was dropped into a suspension of lithium aluminum hydride (0.42 g, 12.0 mmol) in dry ether (40 ml) and stirring was continued for 4 hours at room temperature. Then ice-water was added carefully, and the precipitated aluminum hydroxide was filtered off and washed with ether. The aqueous phase was separated and the organic phase was washed with water, dried over sodium sulfate an evaporated in vacuo to leave an oil (9.0 g) which crystallized spontaneously. Yield: 7.1 g, m.p. 68°-69° C. (from pentane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270334 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-550deb02136e4a33927e2fb8b40d58a3 |
| Source note | uspto-grants-1993_12 |