Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20365471 | HCID 20365471 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20365473 | HCID 20365473 | 92.4% |
Reaction Steps
A mixture of 14.6 g of ethyl 2-[p-(4-tetrahydropyranyl)-phenoxy]-butanoate, 100 ml of ethanol and 40 ml of 2N sodium hydroxide was stirred at 20° C for 24 hours and then refluxed for an hour. The ethanol was evaporated and the residue was taken up in 100 ml of 0.5N sodium hydroxide. The solution was washed with ether and acidified with concentrated hydrochloric acid and was extracted with methylene chloride. The extracts were dried and evaporated to dryness to obtain 13.2 g of raw product which was crystallized from cyclohexane to obtain 12.2 g of 2-[p-(4-tetrahydropyranyl)-phenoxy]-butanoic acid melting at 127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04078076 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-1ad6cc5b47f5473e99ea0dc5003ccfe7 |
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| Source note | uspto-grants-1978_03 |
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