Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Methylisoquinoline | HCID 640959 | 66.5% |
Reaction Steps
Para-tolualdehyde (53 mL, 0.486 mol) was stirred in a solvent of chloroform (900 mL). Aminoacetaldehyde dimethyl acetal (59.3 mL, 0.486 mol) was slowly added thereto, followed by stirring at 90° C. until about one-half of the reaction solution was evaporated. The reaction solution was cooled to room temperature, and the resulting yellow reaction solution was dissolved in chloroform (400 mL), followed by cooling the solution to 0° C. or below. Ethyl chloroformate (48 mL, 0.486 mol) and triethylphosphite (104 mL, 0.583 mol) were slowly added to the reaction solution. The reaction solution was stirred for 24 hours at room temperature. The reaction solution was cooled to 0° C. or below, slowly added with titanium tetrachloride (213.6 mL, 1.94 mol), and refluxed for 12 hours or more. The reaction solution was cooled to room temperature, and stirred for 12 hours or more. The reaction mixture was poured to an ice water to separate the organic layer and the aqueous layer, and the aqueous layer was washed with dichloromethane. A saturated sodium tartrate solution was added to the aqueous layer, adjusted to pH 9 by adding ammonia water, and subjected to extraction with dichloromethane. The obtained organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the title compound (46.3 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156852B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-a587ded8c4e244a19f990846c470ec47 |
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| Source note | uspto-grants-2015_10 |
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