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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10375Generated: October 29, 2026

Acetic Acid → (1R,3S)-3-[2-phenyl-5-methyloxazol-4-ylmethoxy]cyclohexan-1-ol

https://huagongshe.com/reaction/10375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium MethoxideHCID 10942334—
Reactant(1S,3R)-3-[2-phenyl-5-methyloxazol-4-ylmethoxy]cyclohexan-1-olHCID 69539737—
SolventMethanolHCID 887—
Product(1R,3S)-3-[2-phenyl-5-methyloxazol-4-ylmethoxy]cyclohexan-1-olHCID 5868195187.5%

Reaction Steps

0.96 g of the (1R,3S)-acetyl compound from Example 20 was dissolved in approx. 5–10 ml of MeOH, admixed with 0.1 ml of NaOMe (30%) and stirred at 20–23° C. After 3 h, the mixture was neutralized with acetic acid and concentrated under reduced pressure, taken up with ethyl acetate, washed with saturated NaHCO3, dried (MgSO4) and concentrated under reduced pressure. After filtration through silica gel (10:1–0:1 n-heptane/ethyl acetate), 0.84 g of the desired (1R,3S)-3-[2-phenyl-5-methyloxazol-4-ylmethoxy]cyclohexan-1-ol having 95% ee (HPLC on Chiralpak AD 250×4.6; 1 ml/min, 25:1:0.5 heptane/EtOH/CH3CN+0.1% TFA) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094795B2
Source datasetuspto-grants-2006_08
ORD IDord-28284bcf97824fbea3f17da5d93ed400
Source noteuspto-grants-2006_08