- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Automatic Translation feature is available on CiNii Labs
- Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Pd (0Ac)<SUB>2</SUB>-Diphosphine Catalyzed O-Allylation of Alcohols with Allyl Alcoholt
-
- OU Jingping
- Department of Chemistry and Biot echnology, Faculty of Engineering, The University of Tokyo;
-
- ISHIMURA Yoshimasa
- Chemicals Research Laboratory, Showa Denko K. K.;
-
- NAGATO Nobuyuki
- Chemicals Research Laboratory, Showa Denko K. K.;
Bibliographic Information
- Other Title
-
- Pd(OAc)<SUB>2</SUB>-二座配位ホスフイン系触媒を用いたアリルアルコールによるアルコールの O-アリル化反応
- Studies on Allylation on Allyl Alcohol. IV. Pd(OAc)2-Diphosphine Catalyzed O-Allylation of Alcohols with Allyl Alcohol.
Search this article
Description
O-Allylation of alcohols with allyl alcohol catalyzed byPd(OAc)2-diphosphinoalkane was investigated. Pd(OAc)2-dppb[dppb =1, 4-bis (diphenylphosphino) butane] was found to be the most efficient catalyst, and the reaction proceeded effectively in aromatic hydrocarbon solvents such as xylene or toluene under neutral conditions. In the reaction of ethanol and allyl alcohol, the yield of allyl ethyl ether increased from 52% to 89% with increasing the [Ethanol] / [Allyl alcohol] ratio. The selecetivity of allyl ethyl ether was low at the early stage of the reaction, but increased with the progress of the reaction. Allyl ethers of various alcohols were also synthesized in high yields by this Pd(OAc)2-dppb catalyzed O-allylation with allyl alcohol.
Journal
-
- NIPPON KAGAKU KAISHI
-
NIPPON KAGAKU KAISHI 1996 (9), 787-791, 1996-09-10
The Chemical Society of Japan
- Tweet
Keywords
Details 詳細情報について
-
- CRID
- 1390282679365056000
-
- NII Article ID
- 130004061023
-
- ISSN
- 21850925
- 03694577
-
- Data Source
-
- JaLC
- Crossref
- CiNii Articles
-
- Abstract License Flag
- Disallowed