HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562849Generated: October 29, 2026
Diethyl Ether → Benzyl 1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate
https://huagongshe.com/reaction/562849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine | HCID 24229223 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Benzyl 1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate | HCID 58835322 | 50.9% |
Reaction Steps
Into a Round bottom flask was added compound 20 (425.0 mg, 0.001203 mol) and Ether (8.0 mL, 0.076 mol) under an atmosphere of Nitrogen, −78 Celsius. Into the reaction mixture, was added 1.7 M of tert-Butyllithium in Heptane (1.5 mL) slowly. The reaction mixture was stirred at −78 Celsius for 90 minutes, followed by addition of benzyl chloroformate (0.20 mL, 0.0014 mol). 2 hours later at −78 Celsius, the reaction mixture was poured into water, extracted with EtOAc. The organic layer was washed with brine, dried over sodium sulfate, concentrated and purified with biotage to give product 21 (250 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067434B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-11de42fbfea2499ba77b3188cf197ac0 |
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| Source note | uspto-grants-2011_11 |
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