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| | 3-Chloro-2-fluorobenzaldehyde Basic information |
| | 3-Chloro-2-fluorobenzaldehyde Chemical Properties |
| Boiling point | 214 °C (lit.) | | density | 1.35 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.545(lit.) | | Fp | 186 °F | | storage temp. | Inert atmosphere,2-8°C | | form | clear liquid | | color | Light orange to Yellow to Green | | Sensitive | Air Sensitive | | BRN | 5861249 | | InChI | InChI=1S/C7H4ClFO/c8-6-3-1-2-5(4-10)7(6)9/h1-4H | | InChIKey | YAOZCMANASAVFN-UHFFFAOYSA-N | | SMILES | C(=O)C1=CC=CC(Cl)=C1F | | CAS DataBase Reference | 85070-48-0(CAS DataBase Reference) |
| Hazard Codes | Xi,Xn | | Risk Statements | 36/37/38-20/21/22 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29130000 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 3-Chloro-2-fluorobenzaldehyde Usage And Synthesis |
| Chemical Properties | lightyellowliqui | | Uses | 3-Chloro-2-fluorobenzaldehyde is an intermediate used to synthesize small-molecule inhibitors of MDM2-p53 interaction as antitumor agents. It is also used to prepare flavonoid derivatives as selective neuromedin U 2 receptor agonists for obesity treatment. | | Application |
3-Chloro-2-fluorobenzaldehyde is an important fine chemical intermediate used in organic and pharmaceutical synthesis.
| | General Description | 3-Chloro-2-fluorobenzaldehyde is a fluorinated benzaldehyde derivative. | | Hazard | 3-Chloro-2-fluorobenzaldehyde causes skin irritation and serious eye irritation.
| | Synthesis | 36.3 g of sodium bicarbonate and 500 g of dichloromethane were added to a 1 L four-necked flask, followed by 0.5 g of TOMO as a catalyst. The reaction mixture was cooled to 0 to 5°C with stirring. To this cooled mixture was slowly added a mixed solution of 50 g of (3-chloro-2-fluorophenyl)methanol and 100 g of dichloromethane. Next, 230 g of sodium hypochlorite solution was added slowly and dropwise. The reaction mixture was held at 0 to 5°C for 1 hour. The progress of the reaction was monitored by sampling and the reaction was stopped when the content of raw (3-chloro-2-fluorophenyl)methanol was ≤ 1%. After completion of the reaction, the mixture was left to stratify. The organic layer (dichloromethane layer) was separated and the dichloromethane was recovered by simple distillation. Finally, vacuum distillation of the remaining oil layer gave 46.1 g of 3-chloro-2-fluorobenzaldehyde with 97.5% product purity and 91% yield. | | References | [1] Patent: CN104529729, 2016, B. Location in patent: Paragraph 0087; 0088 |
| | 3-Chloro-2-fluorobenzaldehyde Preparation Products And Raw materials |
| Raw materials | 3-CHLORO-2-FLUOROBENZYL ALCOHOL-->TEMPO-->Sodium hypochlorite-->Sodium bicarbonate-->Dichloromethane | | Preparation Products | 3-Chloro-2-fluorobenzoic acid-->(E)-3-chloro-2-fluorobenzaldehyde oxime-->(3S,3'S,4'R,6'R,8'S,8'aR)-6-chloro-8'-(3-chloro-2-fluorophenyl)-6'-(2,2-dimethylpropyl)-3',4'-diphenylspiro[1H-indole-3,7'-4,6,8,8a-tetrahydro-3H-pyrrolo[2,1-c][1,4]oxazine]-1',2-dione-->Benzenemethanamine, 3-chloro-N-cyclopropyl-2-fluoro- |
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