HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289306Generated: October 31, 2026
Toluene → Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oate
https://huagongshe.com/reaction/1289306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 6-bromonaphthalene-2-carboxylate | HCID 1249959 | — |
| Reactant | (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid | HCID 22571498 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oate | HCID 22571563 | — |
Reaction Steps
To a degassed solution of 0.39 g (1.4 mmol) of ethyl 6-bromonaphthalene-2-carboxylate and 3.0 mL of toluene, was added sequentially 49 mg (0.04 mmol) of tetrakis-triphenylphosphine palladium(0), 2.0 mL (2.0 mmol) of 1M sodium carbonate and then a solution of 0.32 g (1.6 mmol) of (5,6,7,8-tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid (Compound B13) in 3.0 mL of MeOH. The reaction was heated at 80° C. for 6 h, diluted with 2N Na2CO3, and extracted with CH2Cl2 (2 x), the organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Flash chromatography (silica, 5% ethyl acetate in hexane) of the crude material gave the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747542 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-4d23b2bb8990472a86339d8efc69e885 |
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| Source note | uspto-grants-1998_05 |
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