HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720966Generated: October 31, 2026
4-Methylbenzyl alcohol → HCID 21890199, compound
https://huagongshe.com/reaction/720966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzyl alcohol | HCID 11505 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 4-(6,7-Dimethoxyquinazolin-4-yloxy)aniline | HCID 11616363 | — |
| Reactant | Toluene triethylamine | HCID 22504574 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21890199 | HCID 21890199 | 51% |
Reaction Steps
4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (129 mg) was added to toluene/triethylamine=10/1 (10 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (193 mg) in methylene chloride was then added to the solution, and the mixture was heated under reflux for 15 min. Subsequently, 4-methylbenzyl alcohol (79 mg) was added thereto, and the mixture was further stirred with heating under reflux for 2 hr. After the completion of the reaction, the reaction solution was allowed to cool to room temperature before distilled water was added thereto. The mixture was subjected to separatory extraction with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution and saturated brine. The washed solution was dried over sodium sulfate and was concentrated, and the residue was purified on a column using chloroform/methanol to give the title compound (108 mg, yield 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135466B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-9c78a7a84354457eab9145a1aac06472 |
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| Source note | uspto-grants-2006_11 |
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