HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725827Generated: October 31, 2026
Dichloromethane → HCID 70205439, compound
https://huagongshe.com/reaction/725827
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzoyl chloride, 3,4,5-trimethoxy- | HCID 78282 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22372113 | HCID 22372113 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 70205439 | HCID 70205439 | 64.2% |
Reaction Steps
A dry dichloromethane solution (5 ml) containing 650 mg of 3,4,5-trimethoxybenzoyl chloride was slowly added dropwise to 5 ml of a pyridine solution containing 520 mg of the crystals obtained in step (7), and stirred at room temperature for 2 hours. After completion of the reaction, a saturated aqueous NaHCO3 solution was added and the reaction mixture was extracted with dichloromethane. The organic layer was collected and washed with a 1N aqueous hydrochloric acid until the pH of the water layer became about 1. The organic layer was allowed to stand for 2 hours, washed with water and a saturated saline solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from dichloromethane-n-hexane to provide 480 mg of the object compound as colorless crystals. Table 2 shows the structure and melting point of the compound obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05707997 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-e99838202452442f8acbd640deded043 |
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| Source note | uspto-grants-1998_01 |
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