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

HRID 2399392Notes

Reaction equation

HRID 2399392 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-34262f963e664b649ca9fc7c12f58f2f
Source dataset
uspto-grants-1995_09
Patent number
US05449690

Reaction notes

Loading…