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Formic Acid → (R)-1-(3-Chlorophenyl)ethanol

HRID 1751900
Notes
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Reaction equation

HRID 1751900 reaction equation
C([O-])=O.[K+].C(O)=O.[Cl:8][C:9]1[CH:10]=[C:11]([C:15](=[O:17])[CH3:16])[CH:12]=[CH:13][CH:14]=1>[Ru].CO>[Cl:8][C:9]1[CH:10]=[C:11]([C@H:15]([OH:17])[CH3:16])[CH:12]=[CH:13][CH:14]=1
ParticipantsConditionsProcedureSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 284Formic AcidHCID 149331-(3-Chlorophenyl)ethanoneHCID 2735122Potassium Formate

Product 1

HCID 6950742(R)-1-(3-Chlorophenyl)ethanolYield 100%

Reagents, catalysts & solvents 2

HCID 23950RutheniumCatalystHCID 887MethanolSolvent

Conditions

Temperature
50 °C

Procedure

A ruthenium complex RuCl[(R,R)-Tsdpen] (mesitylene) (2.1 mg, 0.0033 mmol), potassium formate (1.0 g, 12 mmol), formic acid (138 mg, 3 mmol) and 3′-chloroacetophenone (1.55 g, 10 mmol, substrate/catalyst ratio=3000) were set in a 20 mL glass Schlenk-type reaction tube under an argon atmosphere. Methanol (6 mL) was added thereto and stirred at 50° C. for 24 hours to give (R)-1-(3′-chlorophenyl)ethanol at 100% yield and 96.5% ee optical purity.

Sources & evidence

ORD record
ord-c069fcffd9ad4384ad4742a821f2db62
Source dataset
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09162934B2

Reaction notes

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On this pageParticipantsConditionsProcedureSources & evidenceReaction notes