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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405744Generated: October 31, 2026

Sodium Hydroxide → 2-Phenylhexahydro-2,5-methanopentalene-3a-carboxylic acid

https://huagongshe.com/reaction/2405744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantBromineHCID 24408—
Reactant1-(2-Phenylhexahydro-2,5-methanopentalen-3a-yl)ethanoneHCID 59374956—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-Phenylhexahydro-2,5-methanopentalene-3a-carboxylic acidHCID 67300718—

Reaction Steps

Dioxane (1.81) was added to a solution, cooled to −22° C., of sodium hydroxide (724 g) in water (4.8 l). Bromine (578 g) was metered into this solution such that a temperature of −15° C. was not exceeded. A solution of 1-(2-phenylhexahydro-2,5-methanopentalen-3a-yl)ethanone (290 g) in dioxane (600 ml) was metered into this solution, and the reaction was allowed to warm up gradually to room temperature. tert-Butyl methyl ether was added. Subsequently, water was metered in (2.5 l). After phase separation, the aqueous phase was washed with tert-butyl methyl ether. Subsequently, after addition of tert-butyl methyl ether (5 l), hydrochloric acid (32%) was used to establish a pH of pH 1.5. After phase separation, the organic phase was washed repeatedly with water and clarified with activated carbon. The solvent was changed by distillation under reduced pressure with addition of diisopropyl ether. After extractive stirring with diisopropyl ether at reflux, 2-phenylhexahydro-2,5-methanopentalene-3a-carboxylic acid (292 g) was obtained as a solid with 95% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809325B2
Source datasetuspto-grants-2014_08
ORD IDord-a5b4370320d840ac8341b02b74f56aef
Source noteuspto-grants-2014_08