์ถ์ฒ ์ ํ
๋ถ์
99%
mp
114-116 ยฐC (lit.)
SMILES string
O=C1N(Cc2ccccc2)C(=O)c3ccccc13
InChI
1S/C15H11NO2/c17-14-12-8-4-5-9-13(12)15(18)16(14)10-11-6-2-1-3-7-11/h1-9H,10H2
InChI key
WITXFYCLPDFRNM-UHFFFAOYSA-N
์ผ๋ฐ ์ค๋ช
N-Benzylphthalimide (NBPT), also known as 2-benzylisoindoline-1,3-dione, is an N-substituted phthalimide. It has been prepared by reacting phthalic anhydride with benzyl amine in glacial acetic acid. Vibrational spectra of NBPT has been recorded and assigned. NBPT is a roof-shaped molecule with a planar cyclic imide and a phenyl ring connected by a methylene group. Crystal structure of N-benzylphthalimide has parallel layers of phthalimides stack along the a axis.
์ ํ๋ฆฌ์ผ์ด์
N-Benzylphthalimide may be used in the following syntheses:
- 2-benzyl-1,1,3,3-tetraphenylisoindoline
- tailor-made highly fluorous porphyrin derivatives
- N-benzylisoindole
์ํ ์ฑ์ ์(COA)
์ ํ์ ๋กํธ/๋ฐฐ์น ๋ฒํธ๋ฅผ ์ ๋ ฅํ์ฌ ์ํ ์ฑ์ ์(COA)์ ๊ฒ์ํ์ญ์์ค. ๋กํธ ๋ฐ ๋ฐฐ์น ๋ฒํธ๋ ์ ํ ๋ผ๋ฒจ์ ์๋ โ๋กํธโ ๋๋ โ๋ฐฐ์นโ๋ผ๋ ์ฉ์ด ๋ค์์ ์ฐพ์ ์ ์์ต๋๋ค.
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
์ด๋ฏธ ์ด๋ํ ๊ณ ๊ฐ
The direct conversion of phthalimides to isoindoles.
Journal of Heterocyclic Chemistry, 7(2), 413-413 (1970)
Impact of molecular size on electron spin relaxation rates of nitroxyl radicals in glassy solvents between 100 and 300 K.
Molecular Physics, 105(15-16), 2137-2151 (2007)
Vibrational assignment of N-benzylphthalimide and 15N-benzylphthalimide.
Journal of Molecular Structure, 349, 377-380 (1995)
N-benzylphthalimide.
Acta Crystallographica Section E, Structure Reports Online, 62(6), 2367-2368 (2006)
Highly fluorous porphyrins as model compounds for molecule interferometry.
European Journal of Organic Chemistry, 25, 4823-4833 (2011)
์์ฌ์ ๊ณผํ์ํ์ ์๋ช ๊ณผํ, ์ฌ๋ฃ ๊ณผํ, ํํ ํฉ์ฑ, ํฌ๋ก๋งํ ๊ทธ๋ํผ, ๋ถ์ ๋ฐ ๊ธฐํ ๋ง์ ์์ญ์ ํฌํจํ ๋ชจ๋ ๊ณผํ ๋ถ์ผ์ ๊ฒฝํ์ด ์์ต๋๋ค..
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