HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279743Generated: November 1, 2026
4-Chlorobutyryl chloride → HCID 15512391, compound
https://huagongshe.com/reaction/1279743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | 2-[2-(4-Bromophenyl)propan-2-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole | HCID 15512390 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15512391 | HCID 15512391 | — |
Reaction Steps
A solution of 4-bromo-α,α-dimethyl-α-(4,4-dimethyloxazolin-2-yl)toluene (10.0 g. 0.0338 mole), prepared in accordance with Example 2, in 400 mL THF is cooled to −78° C., n-butyllithium (16 mL, 0.042 mole) is added via syringe, and the mixture is stirred at −78° C. for 30 minutes. While keeping the temperature below −75° C., 4-chlorobutyryl chloride (14.4 g, 0.102 mole) in 30 mL THF is added dropwise, and the mixture is stirred at −78° C. for 30 minutes. The mixture is allowed to warm to −15° C. and is quenched with water. The product is extracted with methylene chloride, washed with saturated NaCl solution, dried over Na2SO4, and concentrated. The residue is cooled to 0° C., treated with minimal acetonitrile, and filtered to afford 4-(4-chloro-1-oxobutyl)-α,α-dimethyl-α-(4,4-dimethyloxazolin-2-yl)toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448406B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-13a08f4c86444e6fa76b032b0821441f |
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| Source note | uspto-grants-2002_09 |
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