HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393451Generated: October 30, 2026
1,3-Dibromopropane → HCID 23384157, compound
https://huagongshe.com/reaction/393451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Methyl cyclopentanecarboxylate | HCID 78365 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 23384157 | HCID 23384157 | 143.3% |
Reaction Steps
To a solution of 1.5 molar LDA in cyclohexane (60 mmol, 40 mL) cooled to −70° C. was added a solution of cyclopentane carboxylic acid methyl ester (42 mmol, 5.6 g) in THF (15 mL) over 30 min. The mixture was stirred for 1 hr at −70° C. Then a solution of 1,3-dibromopropane (60 mmol, 11.9 g) in THF (30 mL) which had been pre-cooled to −70° C. was added all at once and the reaction mixture was stirred at −70° C. for one hr then at room temperature overnight. The reaction mixture was poured into brine (200 mL), the layers were separated, the aqueous layer was extracted with ether (3×30 mL) and the combined organic layers were washed with brine (20 mL), dried (magnesium sulfate) and concentrated to give a yellow oil (15 g). Distillation through a short path apparatus with a 3′ vigreux column gave a yellow oil, 7.96 g (76%), bp 76-80° C. at 0.3 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06806365B2 |
|---|
| Source dataset | uspto-grants-2004_10 |
|---|
| ORD ID | ord-b5e52d2579bb41c1b50fadaf2e24499e |
|---|
| Source note | uspto-grants-2004_10 |
|---|