HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470412Generated: October 29, 2026
Ozone → (S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxyethyl)-6-phenyl-1,3-oxazinan-2-one
https://huagongshe.com/reaction/470412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ozone | HCID 24823 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (R)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one | HCID 59532360 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(2-hydroxyethyl)-6-phenyl-1,3-oxazinan-2-one | HCID 59635684 | 84% |
Reaction Steps
To a solution of (R)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one (3 g, 7.5 mmol) in CH2Cl2 (50 mL) was treated with O3 at −78° C. till the mixture turned blue. Then NaBH4 (285 mg, 75 mmol) was added to the solution at 0° C., and the reaction solution was stirred at room temperature for 3 hours. The reaction was quenched by H2O, and the mixture was extracted with EtOAc. The combined organic phase was concentrated to give the crude product, which was purified by preparative TLC to give (S)-3-((S)-1-(4-bromo-phenyl)ethyl)-6-(2-hydroxyethyl)-6-phenyl-1,3-oxazinan-2-one (2.5 g, 84%). 1H NMR (CDCl3): 1.48 (t, 3H), 2.05-2.41 (m, 4H), 2.71-2.92 (m, 2H), 3.51 (m, 1H), 3.71 (m, 1H), 5.58 (m, 1H), 6.73 (d, 2H), 7.12 (m, 2H), 7.23-7.45 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08629138B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-73e6f9ae71cb410b906ed0417b7e7506 |
|---|
| Source note | uspto-grants-2014_01 |
|---|