Butanoyl chloride, 4-chloro-3-methyl-

Base Information

• Chemical Name: Butanoyl chloride, 4-chloro-3-methyl-
• CAS No.: 63480-13-7
• Molecular Formula: C5H8Cl2O
• Molecular Weight: 155.024
• Hs Code.: 2915907098
• Mol file: 63480-13-7.mol

Synonyms:γ-Chlor-isovalerylchlorid;γ-Chlor-β-methyl-butyrylchlorid;γ-chloro-isovaleryl chloride;4-Chloro-3-methylbutanoyl Chloride;

Chemical Property of Butanoyl chloride, 4-chloro-3-methyl-

Chemical Property:

• PSA: 17.07000
• LogP: 2.01680

Purity/Quality:

97% ^*data from raw suppliers

4-Chloro-3-methylbutanoyl chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Butanoyl chloride, 4-chloro-3-methyl-

There total 5 articles about Butanoyl chloride, 4-chloro-3-methyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

dihydro-4-methyl-2(3H)-furanone (64190-48-3,65284-00-6,70470-05-2,1679-49-8) → 4-chloro-3-methyl-butyryl chloride (63480-13-7)

Guidance literature:

With thionyl chloride; zinc(II) chloride;

Reference yield:

isopentanoyl chloride (108-12-3) → 4-chloro-3-methyl-butyryl chloride (63480-13-7)

Guidance literature:

With chlorine;

Reference yield:

isopentanoyl chloride (108-12-3) → β-chloro-isovaleryl chloride (78584-28-8) + 4-chloro-3-methyl-butyryl chloride (63480-13-7) + 2-chloro-3-methylbutanoyl chloride (35383-59-6)

Guidance literature:

With chlorine; In neat (no solvent); Product distribution; Ambient temperature; liquid phase chlorination of the aliphatic C₅-carboxylic acids and their chlorides, methyl esters and chloromethyl esters, relative reactivity of each hydrogen atoms;

upstream raw materials:

dihydro-4-methyl-2(3H)-furanone

isopentanoyl chloride

chlorine

Downstream raw materials:

γ-Chlor-β-methyl-buttersaeure-diisopropylamid

γ-Chlor-β-methyl-buttersaeure-diisobutylamid