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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954899Generated: November 2, 2026

Sodium Hydroxide → Acetic acid, (6-fluoro-2,3-dihydro-3,3-dimethyl-1H-inden-1-ylidene)-, (2E)-

https://huagongshe.com/reaction/1954899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23293619HCID 23293619—
SolventEthanolHCID 702—
ProductAcetic acid, (6-fluoro-2,3-dihydro-3,3-dimethyl-1H-inden-1-ylidene)-, (2E)-HCID 2329360970%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 2-(6-fluoro-1-hydroxy-3,3-dimethyl-1-indanyl)acetate (16 g, 0.0601 mol) in 1N sodium hydroxide (60.1 ml, 0.0601 mol) and ethanol (60 ml) was stirred for 20 h. The solution was concentrated to a small volume by spin evaporation in vacuo, diluted with deionized water (100 ml), and acidified to pH 3 with 1N hydrochloric acid. This biphasic solution was extracted with dichloromethane (2×100 ml). The extracts were combined, washed with deionized water (20 ml), dried with magnesium sulfate (Mallinckrodt), and concentrated by spin evaporation in vacuo. The residue was dissolved in dichloromethane (30 ml), cooled to 0° C., and diluted with 400 ml of a cold (0° C.) solution of trifluoroacetic acid (45 g, Aldrich) in dichloromethane (400 ml). After 15 min, the solution was concentrated by spin evaporation in vacuo and the residue was crystallized by adding hexanes to give 9.23 g (70%) of (E)-2-(6-fluoro-3,3-dimethyl-1-indanylidene)acetic acid as a white crystalline solid, m.p., 202-203.5° C.:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124284
Source datasetuspto-grants-2000_09
ORD IDord-ff6b0d611950456f830ebbdc068d21ea
Source noteuspto-grants-2000_09