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

HRID 274760Notes

Reaction equation

HRID 274760 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-2e97d8287bca467d8095a8a13555985c
Source dataset
uspto-grants-1995_02
Patent number
US05389683

Reaction notes

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