HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177862Generated: November 1, 2026
Sulfuric Acid → t-Butyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoate
https://huagongshe.com/reaction/2177862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(Furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoic acid | HCID 67108027 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | t-Butyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoate | HCID 67107958 | 119.8% |
Reaction Steps
Concentrated sulphuric acid (0.31 g) was added to a stirred suspension of magnesium sulphate (1.31 g) in DCM (10 ml) in a sealed vial and the mixture was stirred for 5 minutes before addition of a solution of 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoic acid (Intermediate 223, 0.96 g) in DCM (8 ml) and t-butanol (1.03 g). The mixture was stirred in a sealed tube for 48 hours. DCM and saturated aqueous sodium hydrogen carbonate were added to the mixture and the organic layer was separated, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-100%, to give t-butyl 3-(furan-3-yl)-2-methoxy-6-(phenylthiomethyl)benzoate (0.67 g) as a colourless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067905B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-e5858a4945d94139aa33aae9a02e484e |
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| Source note | uspto-grants-2015_06 |
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