Oxalyl chloride → HCID 59424944, compound

HRID 907093Notes

Reaction equation

HRID 907093 reaction equation
[C:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([C:12](O)=[O:13])=[CH:9][CH:10]=2)[N:5]([CH2:15][CH3:16])[CH:4]=1)#[N:2].C(Cl)(=O)C([Cl:20])=O>C(Cl)Cl.CN(C=O)C>[C:1]([C:3]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([Cl:20])=[O:13])=[CH:9][CH:10]=2)[N:5]([CH2:15][CH3:16])[CH:4]=1)#[N:2]

Participants

5

Reactant 2

HCID 65578Oxalyl chlorideHCID 59425917HCID 59425917, compound

Product 1

HCID 59424944HCID 59424944, compoundYield 100.9%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideCatalystHCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

A suspension of 3-cyano-1-ethyl-1H-indole-6-carboxylic acid (0.42 g, 1.96 mmol) in CH2Cl2 (15 mL) was cooled to 0° C. The suspension was treated with DMF (2 drops) and then oxalyl chloride (0.34 mL, 3.92 mmol) was added via syringe during 2 minutes after which the ice bath was removed and the reaction mixture was allowed to warm to ambient temperature during 1.5 h during which time the reaction became a yellow solution. The solution was then concentrated in vacuo to afford 0.46 g (quantitative yield) of 3-cyano-1-ethyl-1H-indole-6-carbonyl chloride as a yellow solid.

Workup

  1. customwas removed
  2. temperatureto warm to ambient temperature during 1.5 h during which time the reaction
  3. concentrationThe solution was then concentrated in vacuo

Sources & evidence

ORD record
ord-9388963416814f7486d79fd21482bf21
Source dataset
uspto-grants-2011_09
Patent number
US08013006B2

Reaction notes

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