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线性分子式:
BF3 · O(C2H5)2
化学文摘社编号:
分子量:
141.93
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
203-689-8
MDL number:
Beilstein/REAXYS Number:
3909607
产品名称
三氟化硼二乙醚,
InChI key
MZTVMRUDEFSYGQ-UHFFFAOYSA-N
InChI
1S/C4H10BF3O/c1-3-9(4-2)5(6,7)8/h3-4H2,1-2H3
SMILES string
CC[O+](CC)[B-](F)(F)F
grade
synthesis grade
vapor density
4.9 (vs air)
vapor pressure
4.2 mmHg ( 20 °C)
form
liquid
expl. lim.
36 %
reaction suitability
core: boron
reagent type: Lewis acid
reagent type: catalyst
refractive index
n20/D 1.344 (lit.)
bp
126-129 °C (lit.)
mp
−58 °C (lit.)
density
1.15 g/mL (lit.)
functional group
ether
storage temp.
2-8°C
Quality Level
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General description
三氟化硼乙醚或三氟化硼乙醚络合物是一种有机化合物,被广泛用作有机合成中便捷的三氟化硼(BF3)源。它也可用作活化亲电子试剂的路易斯酸。
Packaging
建议将25 mL Sure/Seal™ 瓶作为一次性瓶使用。 反复穿刺可能会导致产品性能下降。
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
Application
具有广泛用途的路易斯酸试剂
由芳基环丙酮通过 [3+2] 环加成反应制备环戊基和环庚基[b]吲哚的催化剂。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT RE 1 Inhalation
target_organs
Kidney
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
137.3 °F - closed cup
flash_point_c
58.5 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
European Journal of Organic Chemistry, 5378-5378 (2006)
(1-Alkynyl)dicarbonylcyclopentadienyliron complexes as electron-rich alkynes in organic synthesis: BF3-mediated [2+2] cycloaddition/ring-opening providing (2-alkenyl-1-imino)iron complexes.
Ryotaro Nakaya et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(31), 8559-8561 (2011-06-23)
Meng-Yang Chang et al.
Organic letters, 12(6), 1176-1179 (2010-03-03)
An easy and straightforward synthesis of 6,10b-diarylhexahydrobenzo[f]isoquinoline by the repeated treatment of boron trifluoride etherate (BF(3) x OEt(2)) is reported. The overall transformation from 4-arylpiperidin-3-one to benzo[f]isoquinoline proceeds via ring contraction, chain elongation, and intramolecular electrophilic cyclization in moderate yields.
U C Reddy et al.
The Journal of organic chemistry, 74(6), 2605-2608 (2009-02-17)
A diastereoselective one-pot, three-component Prins-Friedel-Crafts reaction was developed for the synthesis of 4-aryltetrahydropyran derivatives from the reaction of carbonyl compounds with homoallylic alcohol in the presence of arene promoted by boron trifluoride etherate.
Hui Xu et al.
Bioorganic & medicinal chemistry letters, 21(13), 4008-4012 (2011-06-03)
Twenty-one 4α-acyloxy-2-chloropodophyllotoxin derivatives (5a-u), whose C-4 spatial configuration was mainly stereocontrolled by the configuration of C-2 chlorine atom, were unexpectedly prepared by the reaction of 2-chloropodophyllotoxin with carboxylic acids in the presence of BF(3)·Et(2)O. Compared with ordinary esterifications of carboxylic
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