ChemicalBook--->CAS DataBase List--->176980-36-2

176980-36-2

176980-36-2 Structure

176980-36-2 Structure
IdentificationBack Directory
[Name]

(3-FORMYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER
[CAS]

176980-36-2
[Synonyms]

3-(BOC-AMino)benzaldehyde
tert-butyl 3-formylphenylcarbamate
tert-butylN-(3-formylphenyl)carbamate
3-(tert-Butoxycarbonylamino)benzaldehyde
(3-FORMYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER
Carbamic acid, N-(3-formylphenyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C12H15NO3
[MDL Number]

MFCD06660380
[MOL File]

176980-36-2.mol
[Molecular Weight]

221.25
Chemical PropertiesBack Directory
[Melting point ]

88℃
[Boiling point ]

291℃
[density ]

1.163
[Fp ]

130℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

13.50±0.70(Predicted)
[color ]

Beige
[InChI]

1S/C12H15NO3/c1-12(2,3)16-11(15)13-10-6-4-5-9(7-10)8-14/h4-8H,1-3H3,(H,13,15)
[InChIKey]

JEUBPGIHGQWLAJ-UHFFFAOYSA-N
[SMILES]

O=CC1=CC(NC(OC(C)(C)C)=O)=CC=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[RIDADR ]

UN2811
[HS Code ]

2913000090
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

(3-FORMYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER(176980-36-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

BOC-3-AMINOBENZYLALCOHOL

118684-31-4

(3-FORMYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER

176980-36-2

General procedure for the synthesis of tert-butyl (3-formylphenyl)-carbamate from tert-butyl (3-(hydroxymethyl)phenyl)carbamate: activated manganese dioxide (7.8 g, 90 mmol) was added to a solution of dichloromethane (50 mL) containing 3-(tert-butoxycarbonylamino)-benzyl alcohol (2.0 g, 9.0 mmol). The resulting suspension was stirred and reacted at room temperature for 16 hours. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the filtrate was concentrated under reduced pressure to give 1.7 g (85% yield) of the target product. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 9.97 (s, 1H), 7.92 (t, J = 1.8 Hz, 1H), 7.63 (dd, J = 8.0,1.1 Hz, 1H), 7.55 (ddd, J = 7.6,1.4,1.1 Hz, 1H), 7.44 (t, J = 7.6 Hz, 1H), and 1.53 (s, 9H).

[References]

[1] Chemistry - A European Journal, 2016, vol. 22, # 26, p. 8814 - 8822
[2] Angewandte Chemie - International Edition, 2017, vol. 56, # 49, p. 15746 - 15750
[3] Angew. Chem., 2017, vol. 129, p. 15952 - 15957,6
[4] Patent: WO2018/114965, 2018, A1. Location in patent: Page/Page column 27
[5] Chemistry of Materials, 2011, vol. 23, # 21, p. 4844 - 4856
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