HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273795Generated: October 26, 2026
Phosphorus oxychloride → HCID 20093927, compound
https://huagongshe.com/reaction/273795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(chloromethyl)-6-methylquinazolin-4(3H)-one | HCID 135715019 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethyl-p-toluidine | HCID 7471 | — |
| Product | HCID 20093927 | HCID 20093927 | — |
Reaction Steps
2. 114.1 g of 2-chloromethyl-6-methyl-3H-quina-zolin-4-one are dissolved in 1.11 of chloroform and 120 ml of N,N,4-trimethylaniline, treated with 53 ml of phosphorus oxychloride and heated at reflux temperature for 20 h. The reaction mixture is evaporated in a vacuum. The residue is dissolved in 1.0 l of ethyl acetate and washed in succession with 2N hydrochloric acid, water, saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution. The organic extracts are concentrated to about 0.51 in a vacuum. The mixture is left to crystallize at -25° C. overnight. The crystal slurry is filtered, the crystals are washed with ethyl acetate (-25° C.) and dried in a vacuum. 89.9 g of 4-chloro-2-(chloromethyl)-6-methylquinazoline of m.p. 111°-112° C. are obtained. A further 11.1 g of 4-chloro-2-(chloromethyl)-6-methylquinazoline of m.p. 114°-116° C. can be obtained from the mother liquor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387585 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-ec8e685dcf3944b5b17a6d6282cdecb5 |
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| Source note | uspto-grants-1995_02 |
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