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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219846Generated: October 27, 2026

Acetone → sodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoate

https://huagongshe.com/reaction/2219846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium HydroxideHCID 14798—
Reactant(6E)-7-(3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl)-3,5-dihydroxyhept-6-enoic acidHCID 5353627—
SolventMethanolHCID 887—
Productsodium;(E)-7-[3-(4-fluorophenyl)-1-propan-2-ylindol-2-yl]-3,5-dihydroxyhept-6-enoateHCID 1676042562%

Reaction Steps

Fluvastatin (3 g) was completely dissolved in MeOH (15 ml) at reflux temperature. Then, the solution was filtered to obtain a clear solution and heated to reflux again. NaOH (s) (0.29 g) was added at reflux temperature to obtain a precipitate. The slurry was cooled to room temperature to obtain a paste-like mixture. Acetone (30 g) was added dropwise at room temperature and the solution stirred at room temperature for 21 h to obtain a massive precipitate. The product was filtered under nitrogen flow, washed with acetone (2×15 ml) and dried at 50° C. in a vacuum oven for 22.5 h to obtain 1.89 g (62%) of fluvastatin sodium Form XLVIII.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414140B2
Source datasetuspto-grants-2008_08
ORD IDord-f2341bb8e61d4ca48c6469e1f07324c7
Source noteuspto-grants-2008_08