HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78897Generated: October 30, 2026
Dimethyl Sulfoxide → 6-Benzhydryl-dihydropyran-3-one
https://huagongshe.com/reaction/78897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Trans-6-benzhydryl-tetrahydropyran-3-ol | HCID 11608697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Benzhydryl-dihydropyran-3-one | HCID 66631672 | 91% |
Reaction Steps
Into a solution of DMSO (0.13 g, 1.64 mmol) in methylene chloride (5 ml) at −78° C. was added a solution of oxalyl chloride (0.11 g, 0.82 mmol) in methylene chloride (1 ml) in a dropwise manner A solution of trans-2-diphenylmethyl-tetrahydropyran-5-ol 11 (0.2 g, 0.75 mmol) in methylene chloride (2 ml) was added next. The reaction was continued for 15 minutes, triethylamine (0.38 g, 3.73 mmol) was next added portion wise and the reaction mixture was allowed to come to room temperature for over a period of 30 minutes. Additional methylene chloride (10 ml) was added, and washed with sat. aqueous NaHCO3, brine, and then dried over anhydrous Na2SO4. Removal of the solvent and purification by flash chromatography (SiO2, Hexane/Ethyl Acetate 8.5:1.5) gave 2-diphenylmethyl-dihydro-pyran-5-one 12 (0.18 g, 91%) as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08841464B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-38e509f33d164b66b3560617492a9353 |
|---|
| Source note | uspto-grants-2014_09 |
|---|