HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252803Generated: October 26, 2026
3,4,5-Trimethoxybenzaldehyde → Methyl 1-(3,4,5-Trimethoxy-benzyl)-2,3-dihydro-1H-indole-5-carboxylate
https://huagongshe.com/reaction/252803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| Reactant | Dibutyltin dichloride | HCID 12688 | — |
| Reactant | Phenylsilane | HCID 12752 | — |
| Reactant | methyl 2,3-dihydro-1H-indole-5-carboxylate | HCID 21782110 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 1-(3,4,5-Trimethoxy-benzyl)-2,3-dihydro-1H-indole-5-carboxylate | HCID 58930491 | 71% |
Reaction Steps
To a solution of 20 (300 mg, 1.69 mmol), 3,4,5-trimethoxybenzaldehyde (365 mg, 1.86 mmol) and dibutyltin dichloride (51 mg, 0.17 mmol) in THF (8 mL) was added phenylsilane (229 μl, 1.86 mmol). The mixture was stirred overnight at room temperature under nitrogen. Additional aldehyde and phenylsilane were added and the stirring continued until starting material was consumed. THF was evaporated in vacuum and the residue was purified by flash chromatography (eluent 20% EtOAc in hexane). The compound was further purified by re-crystallization in a mixture EtOAc/hexane and finally by a second flash chromatography (eluent 20% EtOAc in hexane) to give the title compound 21 (428 mg, 71%) as a white solid. 1H-NMR (DMSO) δ: 2.96 (t, J=8.4 Hz, 2H); 3.45 (t, J=8.7 Hz, 2H); 3.61 (s, 3H); 3.71 (s, 6H); 3.72 (s, 3H); 4.30 (s, 2H); 6.59 (s, 2H); 6.61 (d, J=8.4 Hz, 1H), 7.54 (d, J=1.6 Hz, 1H); 7.63 (dd, J=1.8, 8.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868205B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-42bd2cd077b54c73947b34af0983135f |
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| Source note | uspto-grants-2011_01 |
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