HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603411Generated: October 31, 2026
Sodium Carbonate → HCID 16110520, compound
https://huagongshe.com/reaction/603411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | HCID 16110430 | HCID 16110430 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 16110520 | HCID 16110520 | 75.6% |
Reaction Steps
To a solution of thiophene-3-boronic acid (53 mg, 0.42 mmol), ethyl {(1S)-5-[3-(4-iodophenoxy)propoxy]-2,3-dihydro-1H-inden-1-yl}acetate (50 mg, 0.10 mmol, Example 94) in toluene (1.8 mL), and 1,4-dioxane (0.45 mL), was added PdCl2(dppf)-CH2Cl2 (7.6 mg, 0.01 mmol), and argon was passed through the mixture for 30 min. Then Na2CO3 (2 N aqueous solution, 0.50 mL) was added, and the mixture was heated to 75° C. for 48 h. The reaction was cooled to rt, and extracted with EtOAc (2×). The combined organic phases were washed with NaHCO3 (saturated aqueous solution), dried, filtered and concentrated under reduced pressure. The residue was purified by preparative thin layer chromatography on silica gel to give 33 mg (73%) of the title compound as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 7.51 (d, 2H), 7.40-7.31 (m, 3H), 7.06 (d, 1H), 6.97 (d, 2H), 6.80 (s, 1H), 6.72 (dd, 1H), 4.24-4.10 (m, 6H), 3.60-3.48 (m, 1H), 2.98-2.90 (m, 2H), 2.72 (dd, 1H), 2.46-2.36 (m, 2H), 2.36-2.23 (m, 2H), 1.85-1.70 (m, 1H), 1.30 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906653B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-0b4780a47c71471e8c2592d1bd7339dd |
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| Source note | uspto-grants-2011_03 |
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