HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 4-Chloro-2-methyl-5,6,7,8-tetrahydroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diethylether water | HCID 21584184 | — |
| Reactant | 4(3H)-Quinazolinone, 5,6,7,8-tetrahydro-2-methyl- | HCID 135431271 | — |
| Catalyst | N,N-Dimethylaniline | HCID 949 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-methyl-5,6,7,8-tetrahydroquinazoline | HCID 19744207 | 95% |
Reaction Steps
To a mixture of 4.5 mL of phosphorus oxychloride and 20 drops of dimethylaniline in 50 mL of toluene was added 4.2 g of 5,6,7,8-tetrahydro-2-methyl-4-quinazolone. The resulting mixture was refluxed for 3 hours and then cooled to room temperature. The reaction mixture was poured into a ice cold aqueous potassium carbonate. After stirring for 5 minutes the mixture was added to diethyl ether/water. The organic layer was recovered washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield a yellow oil. This oil was purified on silica to yield the desired compound as a light yellow solid (4.45 g, 95%): 1H NMR (DMSO-d6, 300 MHz) δ 2.78 (m, 2H), 2.64 (m, 2H), 2.50 (s, 3H), 1.78 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234936 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-5f538b3607604f5e8de28b139735b8bd |
| Source note | uspto-grants-1993_08 |