HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225841Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 54007205, compound
https://huagongshe.com/reaction/2225841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | HCID 53844584 | HCID 53844584 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54007205 | HCID 54007205 | 84.4% |
Reaction Steps
A solution of dimethylsulfoxide (0.079 g) in dichloromethane (2 mL) was added over 20 minutes to a stirred solution of oxalyl chloride (0.123 g) in dry dichloromethane (4 mL) maintained throughout at 178° C. by using an acetone-dry ice bath. After 30 minutes at -78° C., a solution of rac-4-[4-hydroxy-4-(2-naphthalenyl)butoxy]-alpha-oxobenzeneacetic acid methyl ester (0.356 g) in dichloromethane (3 mL) was added over 30 minutes and the reaction mixture was stirred for 30 minutes in the acetone-dry ice bath, then triethylamine (0.144 mL) was added. The cooling bath was removed and the reaction was allowed to equilibrate to room temperature, then water was added and the phases were separated. After the aqueous layer was extracted with dichlormethane (2×7 mL), the combined organic layers were washed with brine, then were dried (MgSO4) and evaporated. The residue was purified by flash chromatography over silica gel (ethyl acetate-hexane; 1:3) and then crystallized from ethyl acetate-hexane to furnish in two crops, 0.299 g of 4-[[4-(2-naphthalenyl)-4-oxobutyl]oxy]-alpha-oxobenzeneacetic acid methyl ester, mp 86°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344843 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-80a71514ca564dc7b2c04253cc64917e |
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| Source note | uspto-grants-1994_09 |
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