Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | HCID 22496314 | HCID 22496314 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58390811 | HCID 58390811 | 44.1% |
Reaction Steps
A suspension of magnesium sulfate (4.61 g, 38.32 mmol) in dichloromethane (37 ml) at 21° C., under N2, was treated with conc H2SO4 (510 μl, 9.58 mmol). After 15 min solid 3-Iodo-5-phenyl-thiophene-2-carboxylic acid (3.7 g, 9.58 mmol) was added followed by t-butanol (4.55 ml, 47.9 mmol) and the flask was stoppered and left over-night for 19.5 h. The reaction mixture was treated with saturated bicarbonate aqueous solution, and filtered. The solid was washed with CH2Cl2 and the filtrate dried and concentrated to an oil. The crude material was purified by flash chromatography using Hexane/CH2Cl2 (3:1) as eluent to give 1.63 g (44%) of 3-Iodo-5-phenyl-thiophene-2-carboxylic acid tert-butyl ester as a colorless solid. NMR 1H (CDCl3, 400 MHz) 7.61-7.59 (m, 2H); 7.43-7.35 (m, 3H), 7.25 (s, 1H), 1.60 (bs, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985769B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-12aa09f0d32b48f3a85891be4eb72063 |
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| Source note | uspto-grants-2011_07 |
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