HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Isoquinolinyloxyacetaldehyde dimethyl acetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Isoquinoline, 1-chloro- | HCID 140539 | — |
| Reactant | 2,2-Dimethoxyethanol | HCID 542381 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Isoquinolinyloxyacetaldehyde dimethyl acetal | HCID 69356950 | 64% |
Reaction Steps
To a stirred suspension of sodium hydride (60% oil dispersion, 1.2 g, 30 mmol) in DMF (6 mL) was added dropwise 2-hydroxyacetaldehyde dimethyl acetal (3.2 g, 30 mmol). The resulting mixture was left to stir for 0.5 h, then a solution of 1-chloroisoquinoline (1.6 g, 10 mmol) in DMF (2 mL) was added and the mixture was stirred at 80° C. for 24 h. The mixture was then poured into water (150 mL) and extracted with ether (2×150 mL). The combined organic extracts were dried over sodium sulfate and evaporated in vacuo. The residue was purified by silica gel chromatography (10% ethyl acetate in hexane) to give 1-isoquinolinyloxyacetaldehyde dimethyl acetal (1.5 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939871B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-c53cdda6ad9d41d5bf99f29db8776956 |
| Source note | uspto-grants-2005_09 |