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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108485Generated: October 30, 2026

Water → HCID 11114441, compound

https://huagongshe.com/reaction/1108485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(6-Methoxynaphthalen-2-yl)propanoyl chlorideHCID 5491692—
ReactantMethyl (+/-)-4-[alpha-hydroxy-5-(1-imidazolyl)-2-methylbenzyl]-3,5-dimethylbenzoateHCID 10882640—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 11114441HCID 11114441100.5%

Reaction Steps

Methyl (±)-4-[α-hydroxy-5-(1-imidazolyl)-2-methylbenzyl]-3,5-dimethylbenzoate (70 g) was suspended in dimethylformamide (350 ml) and pyridine (23.7 ml), and a solution of (S)-2-(6-methoxy-2-naphthyl)propionyl chloride (59.7 g) in toluene (250 ml) was added dropwise to the suspension over 10 minutes with stirring under ice-cooling. The mixture was stirred at room temperature for 4 hours and poured into water (1400 ml). The precipitated oily substance was extracted with toluene and washed successively with 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 113 g of methyl (±)-4-[5-(1-imidazolyl)-α-{(S)-2-(6-methoxy-2-naphthyl)propionyloxy}-2-methylbenzyl]-3,5-dimethylbenzoate as a pale-yellow oil. This was crystallized from ethyl acetate (330 ml) and isopropyl ether (1300 ml) and the obtained crystals were recrystallized from isopropyl alcohol (300 ml) to give 47 g of methyl (S)-4-[5-(1-imidazolyl)-α-{(S)-2-(6-methoxy-2-naphthyl)propionyloxy}-2-methylbenzyl]-3,5-dimethylbenzoate as white crystals, melting point 156-158° C., optical rotation [α]D24 +87.3° (c=1, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066739
Source datasetuspto-grants-2000_05
ORD IDord-d91288b49aa44c10b91a7122758f2ba8
Source noteuspto-grants-2000_05