DIBENZYL CARBONATE

DIBENZYL CARBONATE 구조식 이미지
카스 번호:
3459-92-5
상품명:
DIBENZYL CARBONATE
동의어(영문):
Benzyl carbonate;NSC 406789;DIBENZYL CARBONATE;dibenzyl carbazate;Dibenzylcarbonate,98%;Linezolid Impurity 50;Dibenzyl Carbonate >Dibenzyl carbonate 99%;CARBONIC ACID DIBENZYL ESTER;Carbonic acid, bis(phenylmethyl) ester
CBNumber:
CB5677478
분자식:
C15H14O3
포뮬러 무게:
242.27
MOL 파일:
3459-92-5.mol

DIBENZYL CARBONATE 속성

녹는점
29-33 °C(lit.)
끓는 점
180-190 °C2 mm Hg(lit.)
밀도
1.1515 (rough estimate)
굴절률
1.5485
인화점
>230 °F
용해도
난용성(0.099g/L)(25°C).
물리적 상태
powder to lump
색상
흰색에서 거의 흰색
감도
Air Sensitive
BRN
1882864
CAS 데이터베이스
3459-92-5(CAS DataBase Reference)
EPA
Carbonic acid, bis(phenylmethyl) ester (3459-92-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn
위험 카페고리 넘버 21/22
안전지침서 36
WGK 독일 3
TSCA Yes
HS 번호 29209090
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H312 피부와 접촉하면 유해함 급성 독성 물질 - 경피 구분 4 경고 GHS hazard pictograms P280,P302+P352, P312, P322, P363,P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P321 (…) 처치를 하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
1
2 0

DIBENZYL CARBONATE C화학적 특성, 용도, 생산

화학적 성질

Colorless low melting solid

용도

Ionic liquids can effectively accelerate slow N-benzylation reactions utilizing dibenzyl carbonate as an alkylating reagent. Dibenzyl carbonate (DBzlC) has been used to benzylate phenylacetonitrile, benzyl phenylacetate and phenol. Selective N, N-dibenzylation of primary aliphatic amines was carried with dibenzyl carbonate in the presence of phosphonium salts.

제조 방법

To a stirred solution of benzyl alcohol (0.216 g, 2.00 mol), tributylphosphine (0.303 g, 1.50 mmol), and CyTMG (0.394 g, 2.00 mmol) in DMF (2.00 mL), CO2 was added at room temperature. After 15 min, tetrabromomethane (0.663 g, 2.00 mmol) was added, the reaction vessel was sealed, and the contents were stirred for 2 h. Thereafter, the reaction mixture was diluted with ethyl acetate, washed successively with 0.5 m aqueous HCl and saturated aq. NaHCO3 solution, and dried over Na2SO4. Diphenylmetha- nol was added to the organic solution as an internal standard and the yield of dibenzyl carbonate was determined from the relative integrals of a methylene peak of the carbonate and a methine peak of diphenylmethanol in the 1H NMR spectrum of the ethyl acetate solution. Dibenzyl carbonate, prepared by a larger scale reaction of CO2 with benzyl alcohol (1.08 g, 10.0 mmol), was isolated by column chromatography (cyclohexane/ethyl acetate, 50:1) in 67.3% yield (0.816 g).

일반 설명

Dibenzyl carbonate (DBC) is commonly used as a benzylating agent. Dimethyl carbonate and excess of benzyl alcohol undergoes transesterification in the presence of CsF/α-Al2O3 (cesium fluoride/aluminum oxide) to form DBC. The formation of N,N-dibenzyl derivatives by the reaction of primary aliphatic amines with DBC in the presence of phosphonium salts has been investigated.

DIBENZYL CARBONATE 준비 용품 및 원자재

원자재

준비 용품


DIBENZYL CARBONATE 공급 업체

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