HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307555Generated: November 1, 2026
Sulfuric Acid → Methyl 3'-hydroxy-2,2'-dimethylbiphenyl-4-carboxylate
https://huagongshe.com/reaction/2307555
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-bromo-3-methylbenzoate | HCID 3294148 | — |
| Reactant | 3-Methoxymethoxy-2-methylbenzene-1-boronic acid | HCID 22606935 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Diethylether water | HCID 21584184 | — |
| Product | Methyl 3'-hydroxy-2,2'-dimethylbiphenyl-4-carboxylate | HCID 22606889 | — |
Reaction Steps
1.03 g (5.2 mmol) of 3-methoxymethoxy-2-methylbenzene-1-boronic acid, 1 g (4.4 mmol) of methyl 4-bromo-3-methylbenzoate and 4.4 mL of 2.0M potassium carbonate solution are dissolved in 20 mL of ethylene glycol dimethyl ether. The mixture is degassed using a stream of nitrogen for 10 minutes, and 250 mg (0.22 mmol) of tetrakis(triphenylphosphine)palladium are then added and the medium is stirred for 24 hours at 80° C. After cooling and the usual treatment, the residue obtained is dissolved in 30 mL of methanol and 0.5 mL of sulphuric acid is added. The medium is stirred at room temperature for 6 hours and then poured into an ethyl ether/water mixture. After extraction with ether, the residue is purified by chromatography on silica gel (eluent: 9 heptane/1 ethyl acetate). The desired product is obtained in the form of a thick, colourless oil (m=890 mg; Y=79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831106B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-272dd39cc4c44f76a70ca4c98183a909 |
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| Source note | uspto-grants-2004_12 |
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