Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl chloroformateHCID 10387—
Reactant5-Bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridineHCID 24229223—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventHeptaneHCID 8900—
ProductBenzyl 1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 5883532250.9%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067434B2
Source datasetuspto-grants-2011_11
ORD IDord-11de42fbfea2499ba77b3188cf197ac0
Source noteuspto-grants-2011_11