Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110334Generated: November 2, 2026

Pivalaldehyde → HCID 14553025, compound

https://huagongshe.com/reaction/1110334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
ReactantAmmonium ChlorideHCID 25517—
ReactantIodopyrazineHCID 642841—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 14553025HCID 14553025—

Reaction Steps

A solution of 2-iodopyrazine (1.0 g, 4.85 mmol) in dry diethylether (10 ml) was added to a solution of n-butyl lithium (4.04 ml of 1.5M, 6.06 mmol) in dry diethylether (20 ml) at -50° C. over a period of 5 minutes under a nitrogen atmosphere. This was followed immediately by the addition of a solution of pivaldehyde (0.65 g, 7.58 mmol) in dry diethylether (10 ml). The reaction mixture was allowed to warm to room temperature over 4 hours and then poured into a mixture of ice and 10% ammonium chloride solution. The aqueous solution was extracted with diethylether (3×50 ml). The combined extracts were washed with water, dried over magnesium sulphate and concentrated under reduced pressure. The residue was taken up in diethylether and filtered through a bed of silica gel. The filtrate was concentrated under reduced pressure to give the product as a clear oil. (0.76 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04975112
Source datasetuspto-grants-1990_12
ORD IDord-5ea16f996cc64b7dbd70ccd7f31c6db3
Source noteuspto-grants-1990_12