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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10376Generated: October 27, 2026

Acetic Anhydride → (1R,3S)-3-[2-(4-fluorophenyl)oxazol4-ylmethoxy]cyclohexan-1-ol

https://huagongshe.com/reaction/10376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(Benzyloxy)cyclohexanolHCID 14172789—
ReactantHCID 21980309HCID 21980309—
ReactantMono(3-benzyloxycyclohexyl) glutarateHCID 86594703—
SolventPhosphateHCID 1061—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(1R,3S)-3-[2-(4-fluorophenyl)oxazol4-ylmethoxy]cyclohexan-1-olHCID 12113844—

Reaction Steps

Approx. 10 mg of 3-[2-(4-fluorophenyl)oxazol-4-ylmethoxyl]cyclohexyl acetate (prepared by reacting 3-benzyloxycyclohexan-1-ol with acetic anhydride, in a similar manner to the synthesis of mono(3-benzyloxycyclohexyl) glutarate see Example 39) were taken up in 2 ml of phosphate buffer (0.1 M, pH=7.0) and 2 ml of DME and stirred with approx. 5 mg of Chirazyme L-2, lyo., at 20–23° C. for approx. 20–24 h. The reaction mixture was extracted with dichloromethane. The organic phase was admixed with toluene and concentrated by evaporation under reduced pressure. The determination of the optical purity for (1R,3S)-3-[2-(4-fluorophenyl)oxazol4-ylmethoxy]cyclohexan-1-ol gave 99.4% ee (HPLC on Chiralpak AD 250×4.6; 1 ml/min, acetonitrile) and 98.9% ee for the (1S,3R)-acetate (HPLC on Chiralcel OD 250×4.6; 1 ml/min, 110:5:1 heptane/EtOH/CH3CN+0.1% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094795B2
Source datasetuspto-grants-2006_08
ORD IDord-bdea85ef300d4da788573db5b896a3b8
Source noteuspto-grants-2006_08