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2-fluoro-1-(4-methylphenyl)ethanol

Base Information Edit
  • Chemical Name:2-fluoro-1-(4-methylphenyl)ethanol
  • CAS No.:1446417-88-4
  • Molecular Formula:C9H11FO
  • Molecular Weight:154.184
  • Hs Code.:
  • Mol file:1446417-88-4.mol
2-fluoro-1-(4-methylphenyl)ethanol

Synonyms:2-fluoro-1-(4-methylphenyl)ethanol

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Chemical Property of 2-fluoro-1-(4-methylphenyl)ethanol Edit
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Technology Process of 2-fluoro-1-(4-methylphenyl)ethanol

There total 3 articles about 2-fluoro-1-(4-methylphenyl)ethanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With D-glucose; In aq. phosphate buffer; at 30 ℃; pH=6.5; enantioselective reaction; Microbiological reaction;
DOI:10.1021/acs.orglett.0c01825
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere
1.2: Inert atmosphere; Reflux
2.1: Selectfluor; Candida antarctica lipase B / aq. phosphate buffer / 12 h / 50 °C / pH 7.4 / Enzymatic reaction
3.1: D-glucose / aq. phosphate buffer / 30 °C / pH 6.5 / Microbiological reaction
With Candida antarctica lipase B; D-glucose; sodium hydride; Selectfluor; In tetrahydrofuran; aq. phosphate buffer;
DOI:10.1021/acs.orglett.0c01825
Guidance literature:
Multi-step reaction with 2 steps
1: potassium fluoride; zinc(II) fluoride / acetonitrile / 24 h / 100 °C
2: Rhodococcus ruber alcohol dehydrogenase A overexpressed in E. coli; NADH / isopropyl alcohol / 24 h / 30 °C / pH 7.5 / Enzymatic reaction
With potassium fluoride; zinc(II) fluoride; Rhodococcus ruber alcohol dehydrogenase A overexpressed in E. coli; NADH; In isopropyl alcohol; acetonitrile;
DOI:10.1021/jo400962c
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