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(4-Bromo-thiophen-2-yl)-acetonitrile synthesis

5synthesis methods
18791-75-8 Synthesis
4-Bromothiophene-2-carboxaldehyde

18791-75-8
268 suppliers
$9.00/5g

(4-Bromo-thiophen-2-yl)-acetonitrile

160005-43-6
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79757-77-0 Synthesis
(4-BROMO-2-THIENYL)METHANOL

79757-77-0
101 suppliers
$6.00/1g

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Yield: 96%

Reaction Conditions:

with sodium borohydrid in ethanol;water

Steps:

R.5 [Preparation of 4-Bromothiophene-2-Ylacetonitrile]
Referential Example 5 [Preparation of 4-Bromothiophene-2-Ylacetonitrile] To a solution of 4-bromothiophene-2-carboxaldehyde (9.55 g, 50 mmol, purchased from Aldrich) in 100 ml of ethanol was added sodium borohydride (3.78 g, 100 mmol purchased from Yoneyama Yakuhin) gradually under cooling in an ice bath. After the completion of addition, the mixture was stirred further for 1.5 hours at room temperature. The reaction mixture was acidified with hydrochlorid acid, then was concentrated to dryness under reduced pressure. To the residue was added water and extracted with ether to give 9.29 g (yield: 96%) of 4-bromothiophen-2-ylmethanol as an oil.

References:

Morinaga Milk Industry Co., Ltd. US5589506, 1996, A

18791-75-8 Synthesis
4-Bromothiophene-2-carboxaldehyde

18791-75-8
268 suppliers
$9.00/5g

79757-77-0 Synthesis
(4-BROMO-2-THIENYL)METHANOL

79757-77-0
101 suppliers
$6.00/1g

(4-Bromo-thiophen-2-yl)-acetonitrile

160005-43-6
27 suppliers
inquiry