HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986307Generated: October 29, 2026
Hydrochloric Acid → [[2-[(4-Hydroxyphenyl)thio]ethyl]thio]acetic acid
https://huagongshe.com/reaction/986307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Phenol, 4-[(2-chloroethyl)thio]- | HCID 13576289 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | [[2-[(4-Hydroxyphenyl)thio]ethyl]thio]acetic acid | HCID 14011810 | — |
Reaction Steps
Mercaptoacetic acid (3.5 g, 0.039 mole) was added to ethyl alcohol (100 ml) containing sodium (1.8 g, 0.078 mole). The compound of Example 36 (7.3 g, 0.039 mole) in ethyl alcohol (20 ml) was added dropwise and the mixture refluxed 1 hour. The reaction mixture was cooled to room temperature, poured into water (250 ml) and acidified with 2N hydrochloric acid. The product was extracted into ethyl ether (2×150 ml) and the ethyl ether extracted with 1M sodium bicarbonate (3×80 ml). The combined basic washes were acidified with 2N hydrochloric acid and extracted with ethyl ether (3×150 ml). The combined ethyl ether extracts were washed with water (3×75 ml) and saturated sodium chloride (50 ml), dried over magnesium sulfate, filtered and concentrated to give a yellow solid. Recrystallization from ethyl ether/pentane gave the title compound, m.p. ca. 105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04711903 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-9e5e506fe33c4110b39ecec8fe017f75 |
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| Source note | uspto-grants-1987_12 |
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