Basic information Safety Supplier Related

2-BUTOXYNAPHTHALENE

Basic information Safety Supplier Related

2-BUTOXYNAPHTHALENE Basic information

Product Name:
2-BUTOXYNAPHTHALENE
Synonyms:
  • 2-BUTOXYNAPHTHALENE
  • 2-butoxy-naphthalen
  • butyl 2-naphthyl ether
  • Ai3-20476
  • Einecs 233-998-3
  • Naphthalene, 2-butoxy-
  • Butyl beta-naphthyl ether
CAS:
10484-56-7
MF:
C14H16O
MW:
200.28
EINECS:
233-998-3
Mol File:
10484-56-7.mol
More
Less

2-BUTOXYNAPHTHALENE Chemical Properties

Melting point:
35-36℃
Boiling point:
147-150℃ (4 Torr)
Density 
1.016±0.06 g/cm3(Predicted)
FEMA 
4634 | BUTYL BETA-NAPHTHYL ETHER
storage temp. 
Sealed in dry,Room Temperature
solubility 
Acetonitrile (Slightly), Chloroform (Slightly)
form 
Solid
color 
White to Off-White
Odor
at 100.00 %. sweet fruity floral berry strawberry raspberry
Odor Type
fruity
JECFA Number
2141
LogP
4.96
EPA Substance Registry System
Naphthalene, 2-butoxy- (10484-56-7)
More
Less

2-BUTOXYNAPHTHALENE Usage And Synthesis

Synthesis

109-65-9

135-19-3

10484-56-7

General procedure for the synthesis of 2-butoxynaphthalene from bromobutane and 2-naphthol: 0.14 g (1.0 mmol) of a mixture of 1-naphthol and 2-naphthol was mixed with 1.0 mmol of an alkali metal carbonate (0.14 g of K2CO3 or 0.33 g of Cs2CO3), to which was added in specific cases 11.4 mg (0.05 mmol) of TEBAC and 1.2 mmol of alkyl halide (e.g., 0.14 ml of benzyl bromide, 0.10 ml of ethyl iodide, 0.12 mol of butyl bromide, or 0.11 ml of isopropyl bromide) in a closed vial. The reaction was carried out in a CEM microwave reactor at 20-30 W [or 300 W] for an appropriate time at 125°C. After completion of the reaction, the mixture was dissolved in 25 ml of ethyl acetate and the suspension was filtered. The volatile components were removed by evaporation to give a crude product. The crude product is initially purified by passing through a silica gel layer about 2-3 cm thick, using ethyl acetate as eluent, and analyzed by GC-MS or GC. Similar reactions can be carried out with 3 ml of MeCN as solvent and the post-treatment steps are similar to the solvent-free alkylation described above, but without the addition of ethyl acetoacetate. The major products such as compounds 2, 7, 8, 10a-c and 13a,b were obtained in pure form by repeated chromatography. Control experiments were carried out in a similar manner using benzyl bromide under conventional heating conditions.

References

[1] Chemical Communications, 1998, # 20, p. 2245 - 2246
[2] Letters in Organic Chemistry, 2013, vol. 10, # 5, p. 330 - 336

2-BUTOXYNAPHTHALENESupplier

future industrial shanghai co., ltd
Tel
400-0066400 13621662912
Email
sales@jonln.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
SynAsst Chemical.
Tel
021-60343070
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Email
422131432@qq.com
Shanghai YuLue Chemical Co., Ltd.
Tel
021-60345187 13671753212
Email
lzz841106@aliyun.com