Basic information Safety Supplier Related

Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI)

Basic information Safety Supplier Related

Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI) Basic information

Product Name:
Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI)
Synonyms:
  • Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI)
  • Benzoic acid,3-[[(1,1-diMethylethoxy)carbonyl]aMino]-4-Methoxy-
  • 3-[(tert-Butoxycarbonyl)amino]-4-methoxybenzoic acid, tert-Butyl (5-carboxy-2-methoxyphenyl)carbamate
  • 3-[(tert-butyloxycarbonyl)amino]-4-methoxybenzoic acid
  • 3-(Boc-amino)-4-methoxybenzoic acid
  • 4-methoxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]benzoic acid
CAS:
306937-12-2
MF:
C13H17NO5
MW:
267.28
Product Categories:
  • N-BOC
Mol File:
306937-12-2.mol
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Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI) Chemical Properties

Boiling point:
364.8±32.0 °C(Predicted)
Density 
1.243±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
4.42±0.10(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

HS Code 
29225090
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Benzoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methoxy- (9CI) Usage And Synthesis

Chemical Properties

White powder

Synthesis

24424-99-5

2840-26-8

306937-12-2

General procedure for the synthesis of Boc-3-amino-4-methoxybenzoic acid from di-tert-butyl dicarbonate and 3-amino-4-methoxybenzoic acid: 3-amino-4-methoxybenzoic acid (20.0 g, 119 mmol) was suspended in a solvent mixture of 1 mol/L aqueous NaOH (180 mL) and THF (150 mL). The reaction mixture was cooled in an ice bath. A solution of di-tert-butyl dicarbonate (104.4 g, 479 mmol) in THF (70 mL) was slowly added dropwise under stirring conditions for 30 min. After completion of the dropwise addition, the ice bath was removed and the reaction mixture was continued to be stirred at room temperature for 12 hours. Upon completion of the reaction, THF was removed by distillation under reduced pressure.The remaining aqueous phase was diluted with distilled water and subsequently extracted three times with ethyl acetate (3 × 70 mL). The aqueous phase was acidified to pH 4-5 with concentrated hydrochloric acid and extracted with ethyl acetate (3 × 80 mL). All organic phases were combined, washed with distilled water, and dried over anhydrous sodium sulfate. After filtration, Boc-3-amino-4-methoxybenzoic acid (20.78 g, 65% yield) was obtained as an off-white solid by concentration under reduced pressure, which could be used in the next reaction without further purification.

References

[1] European Journal of Organic Chemistry, 2001, # 2, p. 311 - 322
[2] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 80 - 90
[3] Patent: CN104817489, 2017, B. Location in patent: Paragraph 0037-0040
[4] Patent: US2011/178108, 2011, A1. Location in patent: Page/Page column 17

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