HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25153Generated: October 26, 2026
Bromocyclopentane → Tert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetate
https://huagongshe.com/reaction/25153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | tert-Butyl (4-methylphenyl)acetate | HCID 12362014 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetate | HCID 15234721 | — |
Reaction Steps
33.5 g, (0.3 mol of potassium tert-butoxide are initially introduced into 100 ml of anhydrous DMF at 0° C., and 51.6 g (0.25 mol) of the compound from Example XX in 250 ml of anhydrous DMF are added dropwise. The mixture is stirred at 0° C. for 30 min and 32.2 ml (0.3 mol) of cyclopentyl bromide in 150 ml of anhydrous DMF are added dropwise at 5-15° C. and the mixture is stirred at 25° C. for 20 h. After concentrating, the residue is partitioned between water and diethyl ether, and the ether phase is dried over sodium sulphate and concentrated. The product crystallizes out.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858622B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-f849e1c730c94e5db84ce2e7ae990baa |
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| Source note | uspto-grants-2005_02 |
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