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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191890Generated: November 1, 2026

Sodium Bicarbonate → HCID 59668868, compound

https://huagongshe.com/reaction/2191890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
Reactant(2S,4R)-benzyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-hydroxypyrrolidine-1-carboxylateHCID 59668698—
SolventDichloromethaneHCID 6344—
ProductHCID 59668868HCID 5966886863.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

(2S,4R)-benzyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-hydroxypyrrolidine-1-carboxylate (1.5 g, 3.4 mmol) was added as a solid to a solution of bis(2-methoxyethyl)aminosulfur trifluoride (0.98 mL, 5.1 mmol) in 15 mL CH2Cl2 cooled to −78° C. Reaction was stirred at −78° C. for two hours and then warmed to room temperature and stirred for 2 hours. Reaction was poured into saturated sodium bicarbonate solution and stirred until bubbling ceased. Layers were separated and aqueous layer washed one time with CH2Cl2. Combined organics were washed with brine, dried (MgSO4), filtered, and concentrated to give a yellow oil. The oil was triturated with CH2Cl2 and pentane to yield (2S,4S)-benzyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-fluoropyrrolidine-1-carboxylate JG-20 as a yellow solid (0.96 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329159B2
Source datasetuspto-grants-2012_12
ORD IDord-168726596be74692bac628e8f39ddd42
Source noteuspto-grants-2012_12