![66493-39-8](/CAS/GIF/66493-39-8.gif)
BOC-4-ABZ-OH synthesis
- Product Name:BOC-4-ABZ-OH
- CAS Number:66493-39-8
- Molecular formula:C12H15NO4
- Molecular Weight:237.25
![ETHYL 4-(TERT-BUTOXYCARBONYLAMINO)BENZOATE](/CAS/GIF/110969-44-3.gif)
110969-44-3
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$333.00/5g
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66493-39-8
158 suppliers
$10.00/1g
Yield:66493-39-8 74.5%
Reaction Conditions:
with water;sodium hydroxide in methanol at 25;
Steps:
Synthesis of compound 9
A mixture of compound 8 (300mg, 1.l3mmol) and NaOH (1M, 7mL) in MeOH (5 mL) was stirred at room temperature for overnight. After concentrated, the residue was dissolved in H20, 1 N HC1 was added until pH=2, and the mixture was extracted with EA. The organic layer was washed with brine, dried over Na2SO4 and concentrated to provide the product compound 9(200mg, yield: 74.5%). It was used for the next step without further purification. ‘H NIVIR (DMSO-d6, 400MHz): 12.64 (s, 1H), 9.77 (s, 1H), 7.89(d, 2H, J = 8.4Hz), 7.61 (d, 2H, J = 8.8Hz), 1.54 (s, 9H).
References:
SUZHOU KINTOR PHARMACEUTICALS, INC.;GUO, Chuangxin;TONG, Youzhi WO2017/219800, 2017, A1 Location in patent:Paragraph 00131; 00132
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24424-99-5
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150-13-0
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66493-39-8
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201230-82-2
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inquiry
![TERT-BUTYL N-(4-IODOPHENYL)CARBAMATE](/CAS/GIF/159217-89-7.gif)
159217-89-7
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$6.00/250mg
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66493-39-8
158 suppliers
$10.00/1g
![Di-tert-butyl dicarbonate](/CAS/GIF/24424-99-5.gif)
24424-99-5
833 suppliers
$13.50/25G
![4-(1-HYDROXY-ETHYL)-BENZOIC ACID](/CAS/GIF/97364-15-3.gif)
97364-15-3
44 suppliers
$35.00/100mg
![BOC-4-ABZ-OH](/CAS/GIF/66493-39-8.gif)
66493-39-8
158 suppliers
$10.00/1g
![BOC-4-AMINOBENZYLALCOHOL](/CAS/GIF/144072-29-7.gif)
144072-29-7
90 suppliers
$8.00/250mg
![BOC-4-ABZ-OH](/CAS/GIF/66493-39-8.gif)
66493-39-8
158 suppliers
$10.00/1g