HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892697Generated: October 30, 2026
Oxalyl chloride → HCID 19893089, compound
https://huagongshe.com/reaction/892697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-ISOPROPYL-5-OXOHEXANOIC ACID | HCID 3832573 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19893089 | HCID 19893089 | — |
Reaction Steps
A solution of 6.0 g (0.0468 mole) of oxalyl chloride in 4 ml of benzene was chilled to 0° C under a nitrogen atmosphere. A solution of 4.0 g (0.0234 mole) of 2-isopropyl-5-oxohexanoic acid in 4 ml of benzene was added and the solution was warmed to room temperature, and stirred at room temperature for 20 hours. Evaporation of the solvent under reduced pressure yielded a 2-isopropyl-5-oxohexanoyl chloride residue, and the residue was dissolved in 3 ml of benzene. A 3.1 g (0.0222 mole) quantity of 2-methoxy-4-methylphenol in 5 ml of benzene was added, and the solution was stirred for 20 hours. Ether was added and the solution was washed with water, aqueous saturated sodium chloride, and 5% potassium hydroxide. The organic layer was dried over anhydrous calcium chloride, and the solvent was removed under reduoed pressure to yield a liquid whioh was purified by Kugelrohr distillation bp 120°-125° C./0.04 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05120368 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-fba58a3ca2f74cf3bf36b9171c158160 |
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| Source note | uspto-grants-1992_06 |
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