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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537008Generated: October 29, 2026

Benzaldehyde → (R)-(+)-1-Phenyl-1-propanol

https://huagongshe.com/reaction/537008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant(1S,2R,4R)-1,2-bis((7,7-dimethyl-2-morpholinobicyclo[2.2.1]heptan-1-yl)methyl)disulfaneHCID 86687332—
ReactantHCID 178418750HCID 178418750—
Product(R)-(+)-1-Phenyl-1-propanolHCID 640199—

Reaction Steps

After stirring a mixture of (1S,2R,4R)-1,2-bis((7,7-dimethyl-2-morpholinobicyclo[2.2.1]heptan-1-yl)methyl)disulfane (IIIa) (51 mg, 0.10 mmol) and diethylzinc (3.2 mmol, 1.0 M in hexanes) at ambient temperature for 30 minutes, neat benzaldehyde (200 μL, 2.0 mmol) was added in one portion. Upon complete consumption of benzaldehyde as judged by TLC, sat. aq. NH4Cl (3 mL) was slowly added to the reaction product mixture followed by ethyl acetate (20 mL). The mixture was washed twice with 1 N aq. HCl (20 mL each) and brine (5 mL), dried over solid Na2SO4, and concentrated to give a colorless oil which was purified by silica gel column chromatography (1:10 ethyl acetate/n-heptane) to give (R)-1-phenyl-propanol as a colorless oil (221 mg; 81%; 95.2% e.e.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859765B2
Source datasetuspto-grants-2014_10
ORD IDord-c2ae099410ff41f3af2f6e5316699538
Source noteuspto-grants-2014_10