Triethylamine → 2-(7-Methoxynaphthalen-1-yl)acetonitrile

HRID 2399387Notes

Reaction equation

HRID 2399387 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][C:14]([NH2:16])=O)=[CH:5][CH:4]=1.C(N(CC)CC)C.FC(F)(F)C(OC(=O)C(F)(F)F)=O>O1CCCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][C:14]#[N:16])=[CH:5][CH:4]=1

Participants

5

Procedure

The (7-methoxynaphth-1-yl)acetamide obtained in step E is suspended in 80 cm3 of anhydrous tetrahydrofuran. Triethylamine is added. The solution is cooled in an ice bath, and then trifluoroacetic anhydride is added dropwise, with magnetic stirring.

Workup

  1. temperatureThe solution is cooled in an ice bath

Sources & evidence

ORD record
ord-22402018273349c8af6ddc9b23d2aa6e
Source dataset
uspto-grants-1995_09
Patent number
US05449689

Reaction notes

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