![](/CAS/20200331/GIF/1307231-03-3.gif)
(R)-(4-Bromo-indan-1-yl)-carbamic acid tert-butyl ester synthesis
- Product Name:(R)-(4-Bromo-indan-1-yl)-carbamic acid tert-butyl ester
- CAS Number:1307231-03-3
- Molecular formula:C14H18BrNO2
- Molecular Weight:312.2022
![Di-tert-butyl dicarbonate](/CAS/GIF/24424-99-5.gif)
24424-99-5
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$13.50/25G
![(R)-4-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride](/CAS/20180703/GIF/1307231-02-2.gif)
1307231-02-2
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$116.00/100mg
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1307231-03-3
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Yield:1307231-03-3 91%
Reaction Conditions:
with triethylamine in dichloromethane at 20; for 16 h;
Steps:
V-2 tert-Butyl (R)-(4-bromo-2,3-dihydro-1H-inden-1-yl)carbamate (Compound V-2):
To a solution of compound V-1 (4.7 g 18.91 mmol) in CH2Cl2 (100.0 mL) was added TEA (5.4 g, 52.95 mmol) and BOC2O (5.4 g 24.58 mmol). The resulting mixture was stirred at room temperature for 16 h. After the reaction was completed, the resulting mixture was concentrated under reduced pressure. The residue was purified by flash column chromatography with petroleum ether/ethyl acetate (93/7, v/v) to afford the title compound (5.4 g, 91%) as a light pink solid. LCMS (ESI, m/z): j XM l j =312.1.
References:
WO2020/206000,2020,A1 Location in patent:Paragraph 0187
![4-Bromo-1-indanone](/CAS/GIF/15115-60-3.gif)
15115-60-3
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![(R)-(4-Bromo-indan-1-yl)-carbamic acid tert-butyl ester](/CAS/20200331/GIF/1307231-03-3.gif)
1307231-03-3
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