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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802Generated: October 25, 2026

Acetic Acid → Pivalaldehyde

https://huagongshe.com/reaction/1802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—
ProductPivalaldehydeHCID 12417—
Product2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—

Reaction Steps

In 20 ml of acetic acid was dissolved 2.0 g of 2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol obtained in (1) together with 0.86 ml of trimethylacetoaldehyde. To the solution was added 0.36 g of sodium borohydride under ice-cooling. The reaction mixture was stirred for 30 minutes at room temperature and then subjected to extraction with a mixture of 100 ml of water and 150 ml of ethyl acetate. The ethyl acetate layer was washed with 1N sodium hydroxide, dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to afford 5-bromo-2-neopentylamino-α-(2-pyridyl)benzyl alcohol (2.4 g) as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726306
Source datasetuspto-grants-1998_03
ORD IDord-5873d336793841adad5cbcf873b625c5
Source noteuspto-grants-1998_03