Name | 4-bromobenzaldehyde diethyl acetal |
Synonyms | 4-Bromo-,-Diethoxytoluene 4-bromo-à,à-diethoxytoluene 1-BROMO-4-(DIETHOXYMETHYL)BENZENE 1-bromo-4-(diethoxymethyl)benzene 4-BROMOBENZALDEHYDE DIETHYL ACETAL 4-bromobenzaldehyde diethyl acetal 4-Bromo-alpha,alpha-diethoxytoluene |
CAS | 34421-94-8 |
EINECS | 678-205-5 |
InChI | InChI=1/C11H15BrO2/c1-3-13-11(14-4-2)9-5-7-10(12)8-6-9/h5-8,11H,3-4H2,1-2H3 |
Molecular Formula | C11H15BrO2 |
Molar Mass | 259.14 |
Density | 1.274g/mLat 25°C(lit.) |
Melting Point | 99-101/1mmHg |
Boling Point | 75°C0.2mm Hg(lit.) |
Flash Point | 221°F |
Vapor Presure | 0.00819mmHg at 25°C |
Appearance | Liquid |
Color | Clear colorless to pale yellow |
BRN | 2448775 |
Storage Condition | Argon filled storage |
Sensitive | Easily absorbing moisture |
Refractive Index | n20/D 1.513(lit.) |
MDL | MFCD01863514 |
Hazard Symbols | Xn - Harmful![]() |
Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
HS Code | 29110000 |
application | 4-bromobenzaldehyde diethyl acetal can be used as an organic synthesis intermediate and a pharmaceutical intermediate for laboratory research and development and chemical production. |
preparation | in an absolutely anhydrous instrument, under the protection of nitrogen, cover magnesium chips with 2-methyltetrahydrofuran (10mL), add 4-bromobenzaldehyde, heat to initiate a reaction at 30 ℃, and then drop a solution composed of 4-bromobenzaldehyde and anhydrous 2-methyltetrahydrofuran (40mL), control drop acceleration to keep 35 ℃-40 ℃. After addition, continue the reaction for 1.5h, then cool down to 15 ℃ ~ 20 ℃, and add triethyl orthoformate dropwise within 30 minutes under temperature control conditions. After adding, continue to react at the same temperature for 6 hours. After the reaction is completed, the temperature is reduced to 5 ℃ ~ 7 ℃, 100mL of 10% dilute cold hydrochloric acid is slowly added, the organic layer is separated, the organic layer is washed to neutral 10% sodium carbonate, water is washed, anhydrous sodium sulfate is dried, and the solvent is recovered by distillation to obtain colorless liquid 4-bromobenzaldehyde diethyl acetal. |