4-methoxyphenylboronic acid neopentyl glycol ester

4-methoxyphenylboronic acid neopentyl glycol ester - Names and Identifiers

Name	2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane
Synonyms	4-methoxyphenylboronic acid neopentyl glycol ester 2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane 1,3,2-Dioxaborinane, 2-(4-methoxyphenyl)-5,5-dimethyl- 4-methoxyphenylboronic acid 2,2-dimethyl-1,3-propanediol ester
CAS	213596-33-9

4-methoxyphenylboronic acid neopentyl glycol ester - Physico-chemical Properties

Molecular Formula	C12H17BO3
Molar Mass	220.08
Storage Condition	Room Temprature

4-methoxyphenylboronic acid neopentyl glycol ester - Upstream Downstream Industry

Raw Materials	4-METHOXYPHENYL 4-METHYLBENZENESULFONATE 4-Methoxyphenyl mesylate, 4-[(Methylsulphonyl)oxy]anisole Bis(neopentyl glycolato)diboron 5,5-dimethyl-1,3,2-dioxaborinane 2,2-Dimethyl-1,3-propanediol 4-Chloroanisole
Downstream Products	4,4-Dimethoxybiphenyl

4-methoxyphenylboronic acid neopentyl glycol ester - Introduction

2-(4-Methoxyphenyl)-5,5-dimethy1-1,3,2-dioxaborinane is an organic compound with the chemical formula C12H17BO3. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: White solid
-Molecular weight: 206.08g/mol
-Melting point: 63-64 ° C
-Boiling Point: 280-282 ° C
-Solubility: Slightly soluble in water, soluble in organic solvents such as ethanol, dimethylformamide, etc.

Use:
- 2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane is an important organic boron compound, often used as a catalyst and raw material in organic synthesis.
-It can be used to construct carbon-carbon bonds or carbon-boron bonds, and has a wide range of applications in the fields of synthetic chemistry, pharmaceutical chemistry, Pesticide chemistry and polymer chemistry.

Method:
2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane can be prepared by the following reaction:
1. Phenylboronic acid and neopentyl glycol Ester were obtained as starting materials.
2. Condensation reaction of Phenylboronic acid and neopentyl glycol ester under alkaline conditions.
3. Methanol and catalyst are added, and the reaction is continued to generate 2-(4-methoxyyl) -5,5-dimethy1-1,3,2-dioxaborinane.
4. Finally, the target product is obtained by crystallization or other separation and purification methods.

Safety Information:
2-(4-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane has certain toxicity, so appropriate safety measures need to be taken when using and handling:
-Avoid skin contact, inhalation or ingestion.
-Wear appropriate personal protective equipment such as protective gloves, goggles and protective masks during operation.
-Use in accordance with Good Laboratory Practices and hazardous material management practices.
-The container should be sealed during storage and handling, away from fire and high temperature.
-If accidental exposure or discomfort occurs, seek medical attention immediately.

Last Update：2024-04-09 20:49:11