![142121-93-5](/CAS/GIF/142121-93-5.gif)
4-FLUOROPHENYLGLYCINE-N-BOC PROTECTED synthesis
- Product Name:4-FLUOROPHENYLGLYCINE-N-BOC PROTECTED
- CAS Number:142121-93-5
- Molecular formula:C13H16FNO4
- Molecular Weight:269.27
![Di-tert-butyl dicarbonate](/CAS/GIF/24424-99-5.gif)
24424-99-5
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![4-Fluorophenylglycine](/CAS/GIF/7292-73-1.gif)
7292-73-1
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$10.00/1g
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142121-93-5
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Yield:142121-93-5 99%
Reaction Conditions:
with sodium hydroxide in water;isopropyl alcohol at 20; for 1 h;Cooling with ice;
Steps:
13.1 Step 1. [(tert-Butoxycarbonyl)amino](4-fluorophenyl)acetic acid
Step 1. [(tert-Butoxycarbonyl)amino](4-fluorophenyl)acetic acid To amino(4-fluorophenyl)acetic acid (from Acros, 3.0 g, 18 mmol) in 1.0 M sodium hydroxide in water (25.0 mL, 25.0 mmol), cooled in wet ice bath was added a solution of di-tert- butyldi carbonate (4.6 g, 21 mmol) in isopropyl alcohol (15.0 mL). The ice bath was removed and the resulting suspension was stirred at rt for 1 h. The volatile solvent was removed under reduced pressure and remaining solution was adjusted to pH = 3 with 4M HC1, and then extracted with Ethyl acetate. The organic fraction was washed with brine, dried over sodium sulfate, filtered and concentrated to give 4.75 g (99%) of the desired product, which was used in the next step without further purification.
References:
WO2017/27717,2017,A1 Location in patent:Page/Page column 99
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124-38-9
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![4-FLUOROPHENYLGLYCINE-N-BOC PROTECTED](/CAS/GIF/142121-93-5.gif)
142121-93-5
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153903-23-2
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