HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870397Generated: October 29, 2026
Hydrochloric Acid → Methyl 3-hydroxy-4-(methylthio)benzoate
https://huagongshe.com/reaction/1870397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 3-amino-4-(methylthio)benzoate | HCID 21187837 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-hydroxy-4-(methylthio)benzoate | HCID 21187893 | — |
Reaction Steps
A stirred solution of concentrated hydrochloric acid (3.2 mL) in water (3.6 mL) at from 0° C. to 5° C. is treated with methyl 3-amino-4-(methylthio)benzoate (1.97 g; that is prepared as described in Reference Example 52), followed by a solution of sodium nitrite (0.82 g) in water (2 mL), at such a rate that the temperature remains from 0° C. to 5° C. The mixture is then allowed to warm to room temperature and it is stirred for a further period of 1 hour. The reaction mixture is treated with water (30 mL) and then heated to 55-60° C., until the evolution of nitrogen ceased (4 hours). The mixture is extracted with dichloromethane (2×100 mL) and the combined organic extracts are dried and concentrated. The resulting brown oil is subjected to flash chroma-tography, eluting with a mixture of diethyl ether and pentane (1:4 v/v), to give methyl 3-hydroxy-4-(methylthio)benzoate (0.6 g) in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096768 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-f001d422f7634773bf173c27a647af13 |
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| Source note | uspto-grants-2000_08 |
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