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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212464Generated: October 30, 2026

Trifluoroacetic acid → 2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetal

https://huagongshe.com/reaction/2212464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttrans-4-Decen-1-alHCID 5702654—
SolventMethanolHCID 887—
Product2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetalHCID 21966302—

Reaction Steps

trans-4-Decenal (7.2 g, 46.6 mmol) was mixed with 40 mL (0.37 moL) of aminoacetaldehyde dimethylacetal in 400 mL of methanol and stirred at room temperature for 30 minutes. NaCNBH3 (2.9 g, 46.6 mmol) was added, the reaction was cooled in an ice bath, and 27 mL (0.35 moL) of TFA was added dropwise over 5 minutes. The ice bath was then removed and the reaction was stirred for 70 minutes at room temperature, concentrated to a third of its volume, and partitioned between ethyl acetate (250 mL) and 1N NaOH (200 mL). The organic layer was washed with water (3×75 mL), dried over MgSO4, filtered and concentrated under reduced pressure to yield 11.1 g (45.6 mmol) of 2-(trans-dec-4-en-1-ylamino)acetaldehyde dimethyl acetal as a yellow oil that was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101964B2
Source datasetuspto-grants-2006_09
ORD IDord-b75c278b57f746f7812b6c93df54b916
Source noteuspto-grants-2006_09