HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194001Generated: October 30, 2026
1-Bromo-3-methoxypropane → HCID 66788050, compound
https://huagongshe.com/reaction/2194001
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-methoxypropane | HCID 524551 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylate | HCID 2758812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66788050 | HCID 66788050 | — |
Reaction Steps
To a pre-cooled THF solution (200 ml) under an argon atmosphere was added at −5° C. LDA (2M in THF/heptane/ethylbenzene, 16.24 ml) then dropwise piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (4.4 g, 4.2 ml) in THF (50 ml). The mixture was stirred between −5° C. to 0° C. for 3 hour then 1-bromo-3-methoxypropane (4.97 g) was added slowly at 0° C. The mixture was then stirred overnight at RT, the solvent was evaporated off, the residue taken up in AcOEt and washed with water and brine. The layers were separated, the organic layer dried over sodium sulphate and then evaporated off to give the desired 4-(3-methoxy-propyl)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester a light brown oil (6.058 g) oil that was used in next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329904B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-9eb48f6c4f814fa0a90c83b0e277bb52 |
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| Source note | uspto-grants-2012_12 |
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