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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642071Generated: October 30, 2026

Pivalaldehyde → HCID 57831005, compound

https://huagongshe.com/reaction/1642071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 57830996HCID 57830996—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57831005HCID 57831005—

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Chloro-7-iodo-5-triisopropylsilanyl-5H-pyrrolo[2,3-b]pyrazine (0.56 g, 1.28 mmol) was dissolved in 10 mL of dry tetrahydrofuran and stirred under argon with cooling to −78° C. A solution of isopropylmagnesium chloride with lithium chloride (3 mL, 1M, 3 mmol) was added via syringe. After 10 m, neat pivaldehyde (0.325 mL, 3 mmol, distilled) was added all at once. After 1 h at −78° C., the reaction was quenched by the addition of saturated aqueous ammonium chloride, then diluted with ethyl acetate and allowed to warm to ambient temperature. The organic layer was then washed successively with saturated aqueous sodium bicarbonate and brine. After drying over magnesium sulfate, the solution was filtered and solvent removed, and carried directly into the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119636B2
Source datasetuspto-grants-2012_02
ORD IDord-b98187823657477fb961a75e19c0413f
Source noteuspto-grants-2012_02