HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068206Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 20664169, compound
https://huagongshe.com/reaction/1068206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 20664170 | HCID 20664170 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20664169 | HCID 20664169 | 50.4% |
Reaction Steps
Dimethylsulfoxide (0.121 mL, 1.7 mmol) was added to a solution of oxalyl chloride (0.07 mL, 0.8 mmol) in 10 mL of CH2Cl2 at −78° C. under nitrogen. The reaction mixture was stirred at −78° C. for 20 min., then a solution of dihydro-3-(R)-(3-(R)-(hydroxymethyl)-4-(S)-(3-fluorophenyl)-pyrrolidin-1-yl)-4,4-dimethyl-2(3H)furanone (200 mg, 0.65 mmol) in 1 mL of CH2Cl2 was added. The mixture was stirred at −78° C. for an additional 45 min., then triethylamine (0.46 mL, 3.3 mmol) was added and the cold bath was removed. After the reaction mixture had warmed to room temperature, it was diluted with CH2Cl2 and washed with 1N NaOH and brine. The solution was dried over Na2SO4, filtered and concentrated to afford 100 mg (50% yield) of the title compound. 1H NMR (400 MHz, CDCl3). δ1.17 (s, 3H), 1.24 (s, 3H), 3.08-3.24 (m, 4H), 3.35 (t, 1H, J=8.4 Hz), 3.55 (dd, 1H, J=5.9, 9.6 Hz), 3.66 (dd, 1H, J=7.9, 16 Hz), 3.91 (d, 1H, J=9.0 Hz), 3.98 (d, 1H, J=9.0 Hz), 6.95-6.97 (m, 1H), 7.04 (dt, 1H, J=2.1, 10 Hz), 7.10 (d, 1H, J=7.8 Hz), 7.27-7.32 (m, 1H), 9.71 (d, 1H, J=2.0 Hz). ESI-MS. M/z; (M+H)=306.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248755B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-360f74b6aada44ce8c8aeb975dc03168 |
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| Source note | uspto-grants-2001_06 |
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