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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105761Generated: November 2, 2026

Methanol → cyclohexyl(hydroxy)acetic acid

https://huagongshe.com/reaction/2105761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMandelic AcidHCID 1292—
CatalystRhodiumHCID 23948—
SolventAcetic AcidHCID 176—
Productcyclohexyl(hydroxy)acetic acidHCID 27198980.5%

Reaction Steps

To a solution of 200 mL methanol were added 38.0 g mandelic acid, 2.5 mL acetic acid, and 7.5 g rhodium on carbon (5%, Engelhard 5864). The mixture was sealed in an autoclave, purged with nitrogen, and then filled with hydrogen gas. Hydrogenation was carried out at room temperature for 8 hours at 1400 psi hydrogen. The reaction mixture was then removed from the autoclave and filtered. The filtrate was concentrated and recrystallized from toluene. The colorless crystals were collected by filtration and dried under vacuum to give 31.8 g (80.5%) of racemic 2-cyclohexyl-2-hydroxyacetic acid. 1H NMR (DMSO-d6): δ (ppm) 3.71 (d, 1H), 1.66-1.55 (m, 6H), 1.16-1.09 (m, 5H). 13C NMR (DMSO-d6): δ (ppm) 175.27, 74.19, 41.15, 28.86, 26.74, 25.84, 25.76, 25.57. IR (KBr): ν (cm−1) 3440, 2933, 2856, 1718, 1450, 1280, 1255, 1230, 1103. Anal. Calcd. for C8H14O3: C, 60.74; H, 8.92. Found: C, 61.12; H, 9.28. mp 135-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579429B2
Source datasetuspto-grants-2009_08
ORD IDord-dd55a14fe415469c93bbc508f0dd3b95
Source noteuspto-grants-2009_08