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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449188Generated: October 29, 2026

Acetophenone → 1-Phenylethanol

https://huagongshe.com/reaction/449188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantTriphenylphosphineHCID 11776—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
SolventIsopropanolHCID 3776—
Product1-PhenylethanolHCID 7409—

Reaction Conditions

Temperature30 °C

Reaction Steps

Into a 100-mL stainless-steel autoclave was put 24.0 mg (0.03 mmol) of [CuCl((R,R)-SKEWPHOS)(PPh3)]n obtained in Example 27, triphenyl phosphine of the amount shown in Table 6 below, and 28.8 mg (0.30 mmol) of NaO-t-Bu, followed by replacing with nitrogen in the autoclave, and then 2.0 mL of isopropyl alcohol and 1.05 mL (9.0 mmol) of acetophenone were added. The reaction was carried out with stirring under a hydrogen pressure of 5 MPa at 30° C. for 16 to 17 hours to give 1-phenethyl alcohol which is a hydrogenated compound of acetophenone. The reaction mixture was analyzed by using GC. The results are shown in Table 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481791B2
Source datasetuspto-grants-2013_07
ORD IDord-f73194fae206441abf1fe063a7b64fdc
Source noteuspto-grants-2013_07