HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239036Generated: October 25, 2026
1,4-Dibromobutane → Butyl 1-(4-bromo-butyl)-cyclopentanecarboxylate
https://huagongshe.com/reaction/239036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Butyl cyclopentanecarboxylate | HCID 550335 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Tert-Butyl 1-(4-bromobutyl)cyclopropanecarboxylate | HCID 21932036 | — |
| Product | Butyl 1-(4-bromo-butyl)-cyclopentanecarboxylate | HCID 21932063 | — |
Reaction Steps
Compound 103c was prepared, likewise the procedure described for 103b, starting from butyl cyclopentanecarboxylate (Payne, G. B. et al. J. Org. Chem., 1957, 22, 1680-1682) (80.0 g, 0.42 mol), 1,4-dibromobutane (183.3 g, 0.84 mol) and LDA (2 M in THF/heptane/ethylbenzene, 250 mL, 0.50 mol) to give, after purification by fractional distillation under reduced pressure, 103c (62.8 g, 49%) as a light yellow liquid. bp: T=116-117° C. (p=0.040-0.051 Torr). 1H NMR: δ 4.07 (t, J=6.6 Hz, 2H), 3.38 (t, J=6.8 Hz, 2H), 2.16-2.10 (m, 2H), 1.83 (quintet, J=7.1 Hz, 2H), 1.65-1.59 (m, 8H), 1.50-1.31 (m, 6H), 0.94 (t, J=7.2 Hz, 3H). 13C NMR: δ 177.6, 64.1, 53.9, 38.2, 36.0 (2×), 33.3, 33.0, 30.6, 24.8 (2×), 24.6, 19.1, 13.6. HRMS calcd for C14H25BrO2 (M+): 304.1038, found: 304.1042.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642653B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-a6203147a04941aeb683a77d8d3c129e |
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| Source note | uspto-grants-2014_02 |
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