HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661857Generated: October 29, 2026
Trifluoroacetic acid → 2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetal
https://huagongshe.com/reaction/1661857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | trans-4-Decen-1-al | HCID 5702654 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetal | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030445B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-707c311474664dd8a3e51b5fee52d87e |
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| Source note | uspto-grants-2011_10 |
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