4-Chlorobutanal dimethyl acetal

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CAS:29882-07-3
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CAS:29882-07-3
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CAS:29882-07-3
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Products Intro: Product Name:4-Chlorobutanal dimethyl acetal
CAS:29882-07-3
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4-Chlorobutanal dimethyl acetal Basic information
Product Name:4-Chlorobutanal dimethyl acetal
Synonyms:4-CHLOROBUTANAL DIMETHYL ACETAL;4-CHLOROBUTYRALDEHYDE DIMETHYL ACETAL;4-chloro-1,1-dimethoxybutane;1-Chloro-4,4-dimethoxybutane;4,4-Dimethoxybutyl Chloride;4-Chlorobutanal Dimethyl Acetal 90%;4-Chlorobutyraldehyde Dimethyl Aceta;4-CHLOROBUTANAL DIMETHYL ACETAL (FOR SUMATRIPTAN AND OTHER TRIPTANS),96.0%
CAS:29882-07-3
MF:C6H13ClO2
MW:152.62
EINECS:249-924-8
Product Categories:Other Products;All Aliphatics;Aliphatics
Mol File:29882-07-3.mol
4-Chlorobutanal dimethyl acetal Structure
4-Chlorobutanal dimethyl acetal Chemical Properties
Boiling point 120 °C / 40mmHg
density 1.04
refractive index 1.4270-1.4310
Fp 43°C(lit.)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform, Methanol
form Oil
color Clear Colourless
Stability:Moisture Sensitive
InChIKeyLTLKJYMNUSSFAH-UHFFFAOYSA-N
CAS DataBase Reference29882-07-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 26-36
RIDADR 1993
HazardClass 3.2
PackingGroup III
HS Code 2909199090
MSDS Information
4-Chlorobutanal dimethyl acetal Usage And Synthesis
Chemical PropertiesColorless Liquid
Uses4-Chlorobutanal Dimethyl Acetal 90% is a compound useful in organic synthesis and other chemical processes. It is used as an intermediate in the synthesis of aripiprazole, buspirone, and NAN-190 via reductive alkylation of piperazine derivatives with aldehydes
Synthesis
Methanol

67-56-1

1-Buten-1-ol, 4-chloro-, 1-acetate

763101-16-2

4-Chlorobutanal dimethyl acetal

29882-07-3

Preparation of 4-chlorobutanal dimethanol: 72 g (0.49 mol) of 4-chloro-1-acetoxy-1-butene was dissolved in 300 mL of anhydrous methanol, to which were added 240 g (7.5 mol) of methanol and 15 g of acidic ion exchange resin catalyst treated with macroporous resin 15. The mixture was stirred overnight under reflux conditions and the complete conversion of the E and Z isomers of 4-chloro-1-acetoxy-1-butene to a single high-boiling product, accompanied by a small number of side reactions, was confirmed by GC analysis. Upon completion of the reaction, the mixture was filtered to recover the catalyst and the filtrate was treated with 5 g of solid sodium bicarbonate. Excess methanol was removed by distillation under reduced pressure until the volume was reduced to about 50 mL. The liquid was decanted from the insoluble sodium bicarbonate and distilled through a 6-inch Vigro fractionating column at 25 mm Hg. A colorless fraction with a boiling range of 83-85 °C was collected to give 55.0 g of product (74.4% of the theoretical yield).NMR analysis confirmed the fraction as pure 4-chlorobutanal dimethyl acetal.

References[1] Organic Preparations and Procedures International, 2004, vol. 36, # 5, p. 487 - 490
[2] Patent: US2004/192958, 2004, A1. Location in patent: Page 3
4-Chlorobutanal dimethyl acetal Preparation Products And Raw materials
Raw materialsMethanol-->1-Buten-1-ol, 4-chloro-, 1-acetate
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