2-chloro-4-nitrobenzyl alcohol

2-chloro-4-nitrobenzyl alcohol Suppliers list
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Shanghai civi chemical technology co.,Ltd  
Tel: 86-21-34053660
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Company Name: Shanghai Topbiochem Technology Co., Ltd  
Tel: +86-21-60341587
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Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
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Email: 983544897@qq.com
Company Name: Shanghai Aladdin Bio-Chem Technology Co.,LTD  
Tel: 400-6206333 13167063860
Email: anhua.mao@aladdin-e.com

2-chloro-4-nitrobenzyl alcohol manufacturers

2-chloro-4-nitrobenzyl alcohol Basic information
Product Name:2-chloro-4-nitrobenzyl alcohol
Synonyms:2-chloro-4-nitrobenzyl alcohol;2-Chloro-4-nitrobenzenemethanol;Einecs 257-828-2;Benzenemethanol, 2-chloro-4-nitro-
CAS:52301-88-9
MF:C7H6ClNO3
MW:187.58
EINECS:257-828-2
Product Categories:
Mol File:52301-88-9.mol
2-chloro-4-nitrobenzyl alcohol Structure
2-chloro-4-nitrobenzyl alcohol Chemical Properties
Melting point 83 °C
Boiling point 337.0±27.0 °C(Predicted)
density 1.476±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka13.20±0.10(Predicted)
AppearanceLight yellow to brown Solid
Safety Information
HS Code 2906290090
MSDS Information
2-chloro-4-nitrobenzyl alcohol Usage And Synthesis
Synthesis
METHYL 2-CHLORO-4-NITROBENZOATE

13324-11-3

2-chloro-4-nitrobenzyl alcohol

52301-88-9

General procedure for the synthesis of 2-chloro-4-nitrobenzyl alcohol from methyl 2-chloro-4-nitrobenzoate: In a 250 mL round-bottom flask, methyl 2-chloro-4-nitrobenzoate (5 g, 23 mmol) was dissolved in anhydrous dichloromethane (100 mL). The reaction system was cooled to -78 °C under nitrogen protection. Bis(2-methylpropyl)alumina (35 mL, 35 mmol, 1 M solution in hexane) was added slowly and dropwise. The reaction mixture was kept stirred at -78 °C for 4 h. The reaction was subsequently quenched by the addition of water (5 mL). The reaction mixture was gradually warmed to room temperature over 20 min. Anhydrous sodium sulfate (15 g) was added to dry it. after 10 min, the desiccant was removed by filtration. The filtrate was concentrated under reduced pressure to give 2-chloro-4-nitrobenzyl alcohol in 95% yield.

References[1] Patent: WO2010/132999, 2010, A1. Location in patent: Page/Page column 91
2-chloro-4-nitrobenzyl alcohol Preparation Products And Raw materials
Raw materials2-Chloro-4-nitrobenzoyl chloride-->Methyl 2-chloro-4-nitrobenzoate-->2-Chloro-4-nitrobenzoic acid-->Water-->Hexane-->Dichloromethane
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