DIMETHYL 4-HYDROXYPHTHALATE
DIMETHYL 4-HYDROXYPHTHALATE Basic information
- Product Name:
- DIMETHYL 4-HYDROXYPHTHALATE
- Synonyms:
-
- 4-HYDROXYPHTHALIC ACID DIMETHYL ESTER
- Einecs 245-023-9
- 1,2-diMethyl 4-hydroxybenzene-1,2-dicarboxylate
- Dimethyl 4-hydroxy-1,2-benzenedicarboxylate
- 4-hydroxybenzene-1,2-dicarboxylate
- DIMETHYL 4-HYDROXYPHTHALATE
- 4-hydroxybenzene-1,2-dicarboxylic acid dimethyl ester
- 1,2-Benzenedicarboxylic acid, 4-hydroxy-, 1,2-dimethyl ester
- CAS:
- 22479-95-4
- MF:
- C10H10O5
- MW:
- 210.18
- EINECS:
- 245-023-9
- Mol File:
- 22479-95-4.mol
DIMETHYL 4-HYDROXYPHTHALATE Chemical Properties
- Melting point:
- 110-111℃
- Boiling point:
- 330.6±22.0℃ (760 Torr)
- Density
- 1.284±0.06 g/cm3 (20 ºC 760 Torr)
- Flash point:
- 129.3±15.8℃
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 7.54±0.18(Predicted)
- Appearance
- Off-white to light yellow Solid
DIMETHYL 4-HYDROXYPHTHALATE Usage And Synthesis
Chemical Properties
white solid
Synthesis Reference(s)
Tetrahedron Letters, 18, p. 611, 1977 DOI: 10.1016/S0040-4039(01)92706-6
Synthesis
67-56-1
610-35-5
22479-95-4
General procedure for the synthesis of dimethyl 4-hydroxyphthalate from methanol and 4-hydroxyphthalic acid: 1. thionyl chloride (20 mL) was slowly added to a methanol (100 mL) solution of 4-hydroxyphthalic acid (20 g, 110 mmol). 2. The reaction mixture was stirred at 0 °C, then warmed to 80 °C and held for 4 hours. 3. Upon completion of the reaction, the volatiles were removed by distillation under reduced pressure to give dimethyl 4-hydroxyphthalate (C1-2) as a white solid (23 g, yield: 99%), which could be used in the next step without further purification. 4. 4. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz) and mass spectrometry (ESI): 1H NMR δ 7.77 (d, J = 8.8 Hz, 1H), 7.03 (d, J = 2 Hz, 1H), 6.95 (dd, J = 8.4 and 2.0 Hz, 1H), 3.93 (s, 3H), 3.88 (s, 3H); MS ( ESI) m/z 211 ([M+H]+).
References
[1] Patent: WO2014/18866, 2014, A1. Location in patent: Paragraph 00175; 00176
[2] ChemMedChem, 2010, vol. 5, # 2, p. 213 - 231
[3] Chemistry of Materials, 2014, vol. 26, # 14, p. 4151 - 4162
[4] Patent: US2015/56305, 2015, A1. Location in patent: Paragraph 0270; 0271; 0387; 0388
[5] Chemical Science, 2018, vol. 9, # 24, p. 5312 - 5321
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