HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389403Generated: October 30, 2026
Hydroxyphenylacetic acid → (4-Hydroxyphenyl)propanedioic acid
https://huagongshe.com/reaction/1389403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyphenylacetic acid | HCID 127 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Hydroxyphenyl)propanedioic acid | HCID 3017479 | — |
Reaction Steps
About 0.5 mole of 4-hydroxybenzeneacetic acid is dissolved in about 50 ml of anhydrous tetrahydrofuran at -40° C. To this solution is added 3 equivalents of lithium diisopropylamide. The temperature is maintained at about -40° C. for about 15 minutes. Then 1 equivalent of ethyl chloroformate is added and the temperature is raised from about -40° C. to about 20° C. and the reaction mixture stirred for about 60 minutes. The reaction mixture is poured into water and the monoester of α-carboxy-4-hydroxybenzeneacetic acid is recovered from the aqueous solution. Hydrolysis of the half-ester with sodium hydroxide followed by acidification with hydrochloric acid gives α-carboxy-4-hydroxybenzeneacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04244885 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-adc763570d5144028f4ae482436b039a |
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| Source note | uspto-grants-1981_01 |
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