HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250458Generated: October 25, 2026
Sodium Carbonate → 4-Benzyloxy-1-p-tolyl-isoquinoline-3-carboxylic acid butyl ester
https://huagongshe.com/reaction/250458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | 4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester | HCID 86014503 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyloxy-1-p-tolyl-isoquinoline-3-carboxylic acid butyl ester | HCID 66712754 | 105.8% |
Reaction Steps
4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester (207 mg, 0.5 mmol) and Pd(PPh3)4 (23 mg, 0.02 mmol) were dissolved in THF (3 ml) and the solution was stirred for 10 min before a solution of p-tolylboronic acid (68 mg, 0.5 mmol) in EtOH (0.5 ml) and a solution of Na2CO3 (106 mg, 1 mmol) in water (0.5 ml) were added. The resulting mixture was refluxed with stirring for 4 h. Subsequently, the mixture was concentrated in vacuo. To the residue was added water (2 ml) and the mixture was extracted with EtOAc (10 ml). The organic phase was dried over MgSO4 and evaporated in vacuo to give a yellowish oil (225 mg). Purification by flash column chromatography on silica gel using hexanes:EtOAc=94:6 as the eluent gave the title compound as a colorless oil; MS-(+)-ion: M+1=426.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863292B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-7d780f13eeb849039befe3a570707a91 |
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| Source note | uspto-grants-2011_01 |
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