Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397485Generated: October 31, 2026

Iodine → HCID 68721370, compound

https://huagongshe.com/reaction/1397485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantThiazoleHCID 9256—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68721370HCID 68721370—

Reaction Steps

To a cold (−78° C.) solution of thiazole (0.382 mL, 5.41 mmol) in tetrahydrofuran (30 mL) was added n-butyllithium (3.38 mL, 5.41 mmol, 1.6 M in hexane) dropwise. After 15 minutes, N-boc-3-pyrrolidinone (0.49 mL, 5.41 mmol) was added in a single portion. After 30 minutes, lithium diisopropylamide (5.41 mL, 5.41 mmol, 1.0 M in tetrahydrofuran) was added dropwise. The reaction was allowed to stir for an additional 30 minutes, after which a solution of I2 (1.37 g, 5.4 mmol) in tetrahydrofuran (10 mL) was added dropwise. After 10 minutes, the reaction was then quenched by the addition of saturated aqueous Na2S2O3 (100 mL) and ethyl acetate (100 mL) and allowed to warm to ambient temperature. The layers were separated, and the aqueous was extracted with additional ethyl acetate (2×100 mL). The combined organics were dried with anhydrous Na2SO4, filtered, and concentrated to give a dark solid. The residue was purified by chromatography on SiO2 gel, eluting with 50% ethyl acetate in hexanes, to give the title product as a solid. MS (ESI) m/z 397 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901152B2
Source datasetuspto-grants-2014_12
ORD IDord-a7d71800d3894c4693fd297275f7cd4b
Source noteuspto-grants-2014_12