Ethyl cyanoacetate → HCID 12790932, compound

HRID 1648487Notes

Reaction equation

[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=O.[C:11]([CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])#[N:12]>>[C:11]([C:13](=[C:2]1[CH2:3][C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1]1)[C:14]([O:16][CH2:17][CH3:18])=[O:15])#[N:12]

Participants

Reactant 2

HCID 7764Ethyl cyanoacetate

HCID 119832-Indanone

Product 1

HCID 12790932HCID 12790932, compound

Procedure

Prepared from 2-indanone and ethyl cyanoacetate according to a procedure identical to that used in Stage A of Example 15.

Sources & evidence

ORD record: ord-a236b19e4903468d813ae0020ad2aaaf
Source dataset: uspto-grants-1995_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05436343

Reaction notes

Loading…