HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477121Generated: October 29, 2026
Hydroxyphenylacetic acid → HCID 19974159, compound
https://huagongshe.com/reaction/477121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyphenylacetic acid | HCID 127 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Amino-1-(2-methyl-1,3-thiazol-4-yl)ethanol | HCID 16768496 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19974159 | HCID 19974159 | — |
Reaction Steps
3.16 g (20 mmol) of 2-Hydroxy-2-(2-methyl-thiazol-4-yl)ethanamine are dissolved in 80 ml of absolute tetrahydrofuran and, successively, 3.84 g (20 mmol) of 4-hydroxy-phenylacetic acid, 6.3 g (24 mmol) of triphenylphosphine, 5.6 ml (40 mmol) of triethylamine and 2 ml (20 mmol) of carbon tetrachloride are added. After stirring overnight, the mixture is concentrated, the residue is taken up in 2N hydrochloric acid and the solution is extracted three times with methylene chloride. The aqueous phase is then adjusted to pH 7 with 2N sodium hydroxide solution and evaporated to dryness. The residue from evaporation is extracted by boiling several times with a mixture of chloroform/methanol (1:1). The extracts are concentrated, and the residue is purified on a silica gel column using ethyl acetate/methanol=50:1 as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886814 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-e19665fdf1f64f9e9bcced6e7df99052 |
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| Source note | uspto-grants-1989_12 |
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