HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400077Generated: November 2, 2026
1,3-Dibromopropane → HCID 131732140, compound
https://huagongshe.com/reaction/1400077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | HCID 131732141 | HCID 131732141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131732140 | HCID 131732140 | — |
Reaction Steps
To a solution of Example 48A (21.94 g, 74.4 mmol) in tetrahydrofuran (200 ml) was added dropwise lithium hexamethyl bis(trimethylsilyl)amide (1 M in tetrahydrofuran, 119 mL) at −50° C. The reaction mixture was stirred for 1 hour at the same temperature. 1,3-dibromopropane (150 g, 744 mmol) was added dropwise over 1 hour. The reaction mixture was allowed to warm to −20° C. and stirred at the same temperature for 1 hour. LCMS showed that the reaction was complete. The reaction mixture was quenched with an aqueous ammonium chloride solution (6%, 600 mL), and extracted with ethyl acetate. The organic fraction was washed with aqueous ammonium chloride (6%), brine, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate=80:1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906911B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-8dbb0f56105d479ea5b14452b1ef8bdb |
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| Source note | uspto-grants-2014_12 |
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