tert-Butyl N-(4-iodophenyl)carbamate

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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;(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;N-Boc-4-iodoaniline
CAS:159217-89-7
MF:C11H14INO2
MW:319.14
EINECS:
Product Categories:
Mol File:159217-89-7.mol
tert-Butyl N-(4-iodophenyl)carbamate Structure
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
pka13.12±0.70(Predicted)
AppearanceWhite to off-white Solid
Sensitive Light Sensitive
InChI1S/C11H14INO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
InChIKeyCGALRQWBJFDAKN-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)Nc1ccc(I)cc1
Safety Information
Hazard Codes Xn,N
Risk Statements 22-43-50
Safety Statements 36/37-61
RIDADR UN 3077 9 / PGIII
WGK Germany 3
HS Code 2924297099
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Skin Sens. 1
MSDS Information
tert-Butyl N-(4-iodophenyl)carbamate Usage And Synthesis
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

4-Iodoaniline

540-37-4

TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE

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
tert-Butyl N-(4-iodophenyl)carbamate Preparation Products And Raw materials
Raw materialsN-Boc aniline-->Di-tert-butyl dicarbonate-->4-Iodoaniline
Preparation Products4-Iodo-N,N-dimethyl-Benzenamine-->Boc-4-abz-OH
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