HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387262Generated: October 25, 2026
Triethylsilane → methyl 5-bromo-3-(4-thiepanyl)-1H-indole-7-carboxylate
https://huagongshe.com/reaction/387262
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Thiepan-4-one | HCID 15698157 | — |
| Reactant | methyl 5-bromo-1H-indole-7-carboxylate | HCID 24728848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 5-bromo-3-(4-thiepanyl)-1H-indole-7-carboxylate | HCID 59332706 | 34.3% |
Reaction Steps
To a flask under argon in an ice-bath, the 4-thiepanone (200 mg, 1.536 mmol) in 6 mL of dried CH2Cl2 was first dried w/4 A sieves and then transferred via a double needle tubing (cannula). TMS-OTf (278 uL, 1.536 mmol) was added dropwise and the reaction was stirred for 10 min. A solution of methyl 5-bromo-1H-indole-7-carboxylate (390 mg, 1.536 mmol) in 7 mL of CH2Cl2 was dried with 4 A sieves and then added into above solution dropwise. Stirring continued for 4 hours and the reaction was warmed to room temperature. The mixture was cooled to 0° C. and triethylsilane (245 uL, 1.536 mmol) was added as one portion. The mixture was stirred overnight then warmed to room temperature. The mixture was quenched water and sat. NaHCO3, then diluted water/AcOEt and washed with H2O and brine. 194 mg of crude product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372875B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-66a71348ceb742b7a75b84aee0a3e8f2 |
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| Source note | uspto-grants-2013_02 |
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