Pan, En-De et al. published their research in Gaodeng Xuexiao Huaxue Xuebao in 2003 | CAS: 120121-01-9

(R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Quality Control of (R)-1-(3-Chlorophenyl)ethanol

Highly enantioselective transfer hydrogenation of aromatic ketones was written by Pan, En-De;Li, Yan-Yun;Dong, Zhen-Rong;Chen, Jian-Shan;Li, Bao-Zhu;Zhang, Hui;Gao, Jing-Xing. And the article was included in Gaodeng Xuexiao Huaxue Xuebao in 2003.Quality Control of (R)-1-(3-Chlorophenyl)ethanol This article mentions the following:

Enantioselective reduction of prochiral ketones with 2-propanol or formic acid catalyzed by chiral metal complexes has been developed as a synthetic method complementary to asym. hydrogenation in the past decade. However, these processes are necessary to be improved for practical use in organic synthesis because of low catalytic activity and insufficient enantioselectivity. In this paper, we report an excellent catalytic system generated in situ from iridium complex IrCl(Ph3P)3 and chiral tetradentate diaminodiphosphine ligand for asym. transfer hydrogenation of various aromatic ketones. For isobutyrophenone transfer hydrogenation, the corresponding optically active alc. was obtained in 93% yield and with up to 99% e. e. after 5 h at 28 °C. Propiophenone was a better substrate with respect to catalytic activity and enantioselectivity in the presence of base as a co-catalyst. The conversion of propiophenone reached 95.8% and the turnover number as high as 3 193 h-1. These results will provide a useful index for further designing practical chiral catalytic systems. In the experiment, the researchers used many compounds, for example, (R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9Quality Control of (R)-1-(3-Chlorophenyl)ethanol).

(R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Quality Control of (R)-1-(3-Chlorophenyl)ethanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts