에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트

에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트
에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트 구조식 이미지
카스 번호:
71301-98-9
한글명:
에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트
동의어(한글):
에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트
상품명:
Ethyl (R)-(+)-2-(4-hydroxyphenoxy)propionate
동의어(영문):
(R)-ethyl 2-(4-hydroxyphenoxy)propanoate;Ethyl 2(R)-(4-Hydroxy-phenoxy)-propionate;Ethyl(R)-(+)-2-(4-hydroxyphenoxy)propanoate;(R)-2-(p-Hydroxyphenoxy)propionic acid ethyl ester;(R)-2-(4-Hydroxyphenoxy)propionic acid ethyl ester;Propanoic acid, 2-(4-hydroxyphenoxy)-, ethyl ester, (2R)-
CBNumber:
CB41126914
분자식:
C11H14O4
포뮬러 무게:
210.23
MOL 파일:
71301-98-9.mol

에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트 속성

녹는점
36-37℃
끓는 점
327℃
밀도
1.156
인화점
124℃
저장 조건
2-8°C
산도 계수 (pKa)
10.09±0.15(Predicted)

안전

에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트 C화학적 특성, 용도, 생산

Synthesis

Ethyl (R)-(+)-2-(4-hydroxyphenoxy)propionate is prepared by the reaction of hydroquinone and (R)-ethyl O-bezenesulfonyl lactate in the presence of inert atmosphere. The steps are as follows:
Add hydroquinone (8.25g, 0.075mol), sodium carbonate (6.36g, 0.06mol), PEG-1500 (0.5g) into a 250mL nitrogen-proof flask equipped with a magnetic stir bar, and pass the nitrogen-proof flask into The nitrogen is then pumped with an oil pump and then fed into nitrogen (three consecutive times), and then 80 mL of xylene is added, and the reaction flask is placed in an oil bath heated to 120°C for 1 hour.Then add dropwise the xylene dilution liquid of ethyl lactate benzenesulfonate (12.9g, 0.05mol/20ml xylene, add three times, add once in 10 minutes, and add the next in 30 minutes), and then react after the addition is complete. The 6h reaction is over; the reaction solution is suction filtered, an appropriate amount of water is added to the suction filtrate, the solution is extracted with dichloromethane (washed and separated three times), dried with anhydrous sodium sulfate, and finally the solvent is removed by a rotary evaporator to obtain a light yellow Transparent crystals (containing a small amount of hydroquinone), 9.1 g of Ethyl (R)-(+)-2-(4-hydroxyphenoxy)propionate was obtained by column chromatography, and the yield was 86.7%. Where Ar represents that the reaction system is always isolated from oxygen, that is, inert gas protection is used.
Ethyl (R)-(+)-2-(4-hydroxyphenoxy)propionate synthesis

에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트 준비 용품 및 원자재

원자재

준비 용품


에틸(R)-(+)-2-(4-히드록시페녹시)프로피오네이트 공급 업체

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