Synthesis of 2,4-dichlorobenzaldehyde

Preparation of 2,4-dichlorobenzaldehyde

The 2,4-dichlorobenzal chloride (or 2,4-dichlorobenzal bromide) is stirred with eight times its weight of concentrated sulfuric acid in a three-necked flask with a ground sleeve, stirrer, reflux condenser, and a wide capillary serving as gas-inlet tube. Nitrogen is passed in through the capillary, and simultaneously the vacuum of a water pump is applied to the upper end of the reflux condenser. A vigorous evolution of hydrogen chloride (or hydrogen bromide) takes place at 90-110°C. The reaction mixture changes the color to an intense red-brown color and the evolution of hydrogen chloride (or hydrogen bromide) ceases after about 1-2 hours. Then the mixture is poured on to ice and the 2,4-dichlorobenzaldehyde formed is extracted several times with ether, the ethereal extracts are neutralized with sodium bicarbonate solution and then washed with water and dried over magnesium sulfate. After evaporation of the ether, the residue is distilled in vacuo or recrystallized from ligroin. The yield of 2,4-dichlorobenzaldehyde is 80%, m.p. 69-71 °C; b.p. 233 °C.

Organicum. Practical Handbook of Organic Chemistry, by Heinz Becker, Werner Berger and Günter Domschke, Addison-Wesley Pub. Co, 203-204, (1973)





InChI Key


Canonical SMILES


Depositor-Supplied Synonyms

2,4-DICHLOROBENZALDEHYDE, 874-42-0, Benzaldehyde, 2,4-dichloro-, 2,4-dichloro-benzaldehyde, CCRIS 6013, YSFBEAASFUWWHU-UHFFFAOYSA-N, NSC 8762, EINECS 212-861-1, AI3-16063, AH-034/32850055, NSC8762, ACMC-209qnb, DSSTox_CID_2130, 2,4 dichloro benzaldehyde, 2,4-di-chlorobenzaldehyde, 2,4-dichloro benzaldehyde, AC1L21NL, AC1Q3I5T, DSSTox_RID_76500, DSSTox_GSID_22130, SCHEMBL95435, KSC448O3H, UNII-Z08QL2124R, 1,3-Dichloro-4-formylbenzene, 146757_ALDRICH, 2,4-bis(chloranyl)benzaldehyde, 2,4-DCAD, CHEMBL1531235, 35250_FLUKA, CTK3E8733, (2,4-dichlorophenyl)formaldehyde, MolPort-000-871-207, Z08QL2124R, ZINC478344, NSC-8762, Tox21_201217, ANW-38805, BBL023701, SBB040230, STK299308, ZINC00478344, AKOS000118972, LS-1876, MCULE-7304210339, PS-6004, RP23688, RTR-038116, NCGC00091704-01, NCGC00091704-02, NCGC00258769-01, AC-11246, AJ-23092, AK-77305, AN-20568, CAS-874-42-0, CJ-04283, KB-17435, OR034616, P729, SC-23165, ZB014131, AB1002778, DB-076953, KB-225497, ST2415784, TR-038116, D0330, FT-0610037, ST45169250, T8239, 78648-EP2284157A1, 78648-EP2298731A1, 78648-EP2305629A1, 78648-EP2308847A1, A842216, 3B4-3546, I14-7352, W-104022, InChI=1/C7H4Cl2O/c8-6-2-1-5(4-10)7(9)3-6/h1-4

Removed Synonyms

Benzaldehyde,4-dichloro-, C7H4Cl2O, CID13404

Share This

Leave a Reply

Your email address will not be published. Required fields are marked *