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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(2-Phenylhexahydro-2,5-methanopentalen-3a-yl)ethanone | HCID 59374956 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Phenylhexahydro-2,5-methanopentalene-3a-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809325B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-a5b4370320d840ac8341b02b74f56aef |
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| Source note | uspto-grants-2014_08 |
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