HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255261Generated: October 29, 2026
Triethylamine → 5-(2-(Tert-butyldimethylsilyloxy)ethyl)thiophene-3-carbaldehyde
https://huagongshe.com/reaction/1255261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(2-(Tert-butyldimethylsilyloxy)ethyl)-2-chlorothiophene-3-carbaldehyde | HCID 57989211 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-(Tert-butyldimethylsilyloxy)ethyl)thiophene-3-carbaldehyde | HCID 57988903 | — |
Reaction Steps
A slurry of palladium on carbon (10%, 0.28 g) in water (0.5 mL) was added cautiously to a solution of 5-(2-(tert-butyldimethylsilyloxy)ethyl)-2-chlorothiophene-3-carbaldehyde [Aromatic Intermediate 17, step b] (0.80 g) and triethylamine (0.91 mL) in ethanol (50 mL) and the resulting mixture stirred overnight under 4 bar pressure of hydrogen. The mixture was filtered through Celite and the filter pad washed with ethanol (10 mL). The combined filtrate and washings were evaporated and azeotroped with toluene (20 mL) to give a yellow oil. The residue was dissolved in DCM (100 mL), manganese dioxide (2.28 g) was added and the resulting suspension heated at reflux overnight. The mixture was filtered through Celite and the filter pad washed with DCM (50 mL). The combined filtrate and washings were evaporated to give the titled compound as a yellow oil. Yield 0.60 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455483B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-878ffb4abf7e45cc82021f2c0d83c49b |
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| Source note | uspto-grants-2013_06 |
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