HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108487Generated: October 30, 2026
Methyl (+/-)-4-[alpha-hydroxy-5-(1-imidazolyl)-2-methylbenzyl]-3,5-dimethylbenzoate → HCID 69548778, compound
https://huagongshe.com/reaction/1108487
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl (+/-)-4-[alpha-hydroxy-5-(1-imidazolyl)-2-methylbenzyl]-3,5-dimethylbenzoate | HCID 10882640 | — |
| Reactant | HCID 42259206 | HCID 42259206 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 69548778 | HCID 69548778 | 100.3% |
Reaction Steps
Methyl (±)-4-[α-hydroxy-5-(1-imidazolyl)-2-methylbenzyl]-3,5-dimethylbenzoate (9.2 g) was suspended in dichloroethane (110 ml) and pyridine (3.15 ml), and a solution of (S)-2-(4-chlorobenzenesulfonylamino)propionyl chloride (8.9 g) in dichloroethane (25 ml) was added dropwise over 5 minutes with siring under ice-cooling. The mixture was sired at room temperature for 3 hours and the reaction mixture was washed successively with water, 5% citric acid, 5% potassium carbonate and water. The organic layer was separated and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give 15.7 g of methyl (±)-4-[5-(1-imidazolyl)-α-{(S)-2-(4-chlorobenzenesulfonylamino)propionyloxy}-2-methylbenzyl]-3,5-dimethylbenzoate as a pale-yellow oil. This was crystallized from ethyl acetate (27 ml) and isopropyl ether (108 ml) and the obtained crystals were recrystallized from ethyl acetate (15 ml) and isopropyl ether (30 ml) to give 5.2 g of methyl (S)-4-[5-(1-imidazolyl)-α-{(S)-2-(4-chlorobenzenesulfonylamino)propionyloxy}-2-methylbenzyl]-3,5-dimethylbenzoate as white crystals, melting point 126-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06066739 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-bf71fc9f24f443188aaefc70702fe0a0 |
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| Source note | uspto-grants-2000_05 |
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