TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE Basic information
- Product Name:
- TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
- Synonyms:
-
- N-(tert-Butoxycarbonyl)-4-iodoaniline
- N-BOC-4-IODOANILINE
- TERT-BUTYL 4-IODOPHENYLCARBAMATE
- TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE
- (4-Iodophenyl)carbamic acid tert-butyl ester
- N-(4-iodophenyl)carbamic acid tert-butyl ester
- Carbamic acid, N-(4-iodophenyl)-, 1,1-dimethylethyl ester
- ert-Butyl(4-iodophenyl)carbamate
- CAS:
- 159217-89-7
- MF:
- C11H14INO2
- MW:
- 319.14
- Mol File:
- 159217-89-7.mol
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE Chemical Properties
- Melting point:
- 144-148 °C
- Boiling point:
- 299.0±23.0 °C(Predicted)
- Density
- 1.591±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- solid
- pka
- 13.12±0.70(Predicted)
- Appearance
- White to off-white Solid
- Sensitive
- Light Sensitive
TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE Usage And Synthesis
Synthesis
24424-99-5
540-37-4
159217-89-7
GENERAL STEPS: The reaction was carried out in a 50 mL round-bottomed flask at 80°C under reduced pressure for 10 minutes. In a typical experiment, 5 mmol of p-iodoaniline was mixed with 5 mmol of di-tert-butyl dicarbonate and the reaction lasted for 10 minutes. Upon completion of the reaction, the solvent was removed by rotary evaporator under vacuum to give tert-butyl (4-iodophenyl)carbamate.
References
[1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 22, p. 5864 - 5869
[2] Research on Chemical Intermediates, 2017, vol. 43, # 3, p. 1355 - 1363
[3] Chemical Communications, 2013, vol. 49, # 61, p. 6909 - 6911
[4] Patent: WO2004/12736, 2004, A1. Location in patent: Page/Page column 24
[5] Organic Letters, 2018, vol. 20, # 7, p. 1693 - 1697
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TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE(159217-89-7)Related Product Information
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