HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537008Generated: October 29, 2026
Benzaldehyde → (R)-(+)-1-Phenyl-1-propanol
https://huagongshe.com/reaction/537008
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | (1S,2R,4R)-1,2-bis((7,7-dimethyl-2-morpholinobicyclo[2.2.1]heptan-1-yl)methyl)disulfane | HCID 86687332 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Product | (R)-(+)-1-Phenyl-1-propanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859765B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c2ae099410ff41f3af2f6e5316699538 |
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| Source note | uspto-grants-2014_10 |
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