HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854582Generated: October 30, 2026
tert-Butyl acetate → Tert-butyl 2-(2-chloro-5-isopropyl-phenyl)acetate
https://huagongshe.com/reaction/1854582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 3-Bromo-4-chloroisopropylbenzene | HCID 50997864 | — |
| Catalyst | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Tert-butyl 2-(2-chloro-5-isopropyl-phenyl)acetate | HCID 117720579 | 90.4% |
Reaction Steps
Add bis(dibenzylideneacetone)palladium (49.2 mg, 85.6 μmol) to a round bottom flask and seal with a septum. Flush with nitrogen. Add tri-tert-butylphosphine (85.6 μL, 85.6 μmol, 1M in toluene) and lithium bis(trimethylsilyl)amide (12.8 mL, 11.56 mmol, 0.9M in methylcyclohexanes) via a syringe. Add 2-bromo-1-chloro-4-isopropyl-benzene (1.0 g, 4.28 mmol) and t-butyl acetate (865.2 μL, 6.42 mmol) via a syringe. Add toluene (10.7 mL) via a syringe and the reaction mixture becomes hot to the touch. Place on an ambient temperature water bath and stir for 3 hours. Store the reaction mixture in the freezer over the weekend. Warm the reaction mixture to ambient temperature. Dilute the reaction mixture with diethyl ether and add saturated ammonium chloride solution. Separate the layers and wash the diethyl ether layer with saturated sodium chloride solution. Dry over sodium sulfate, filter and concentrate under reduced pressure. Purify the residue by silica gel chromatography eluting with acetone: hexanes (0-2% gradient) to give the title compound (1.04 g). Purify again by silica gel chromatography eluting with dichloromethane: hexanes (0-20% gradient) to give the title compound (490 mg, 1.82 mmol). MS (m/z): 213.0 (M-tBu+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962654B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4f15eebe23404caf92548f6ab4a0f95c |
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| Source note | uspto-grants-2015_02 |
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