HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268500Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 18348548, compound
https://huagongshe.com/reaction/2268500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18348532 | HCID 18348532 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18348548 | HCID 18348548 | 99% |
Reaction Steps
To a solution of oxalyl chloride (0.394 ml) in THF (36 ml) was dropwise added a solution of dimethylsulfoxide (468 mg) in THF (2.4 ml) at −70° C. or under nitrogen atmosphere. After the reaction mixture was stirred for 10 min, a solution of 8-(4,5,6,7-tetramethoxy-2-phenylindan-2-yl)octanol (1.00 g) in THF (12 ml) was dropwise added to the reaction mixture at −70° C. or under. After being stirred for 15 min, the reaction mixture was stirred at between −60° C. and −50° C. for 1 hr, to which triethylamine (2.30 ml) was dropwise added. The reaction mixture was allowed to warm to 0° C. and stirred for 20 min, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo. The residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate=4:1) to yield the entitled compound (985 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326369B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-790c688c75a1436886379cf10d82dad4 |
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| Source note | uspto-grants-2001_12 |
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