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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086518Generated: November 4, 2026

1-Bromo-3-chloropropane → HCID 69482970, compound

https://huagongshe.com/reaction/2086518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantHCID 4649960HCID 4649960—
SolventMethanolHCID 887—
ProductHCID 69482970HCID 69482970800.7%

Reaction Conditions

Temperature65 °C

Reaction Steps

N-decylpiperidine was synthesized by reacting 45.7 g of piperidine with 118.7 g of 1-bromodecane in 237 mL of acetone in the presence of 74 g of potassium carbonate. After refluxing this reaction mixture at 55° C. for 24 hr, it was filtered and acetone was removed from the filtrate to yield 61 g of N-decylpiperidine. N-decylpiperidine (5 g) and 42 g of 1-bromo-3-chloropropane were dissolved in 50 mL of methanol and the reaction mixture was heated to 65° C. for 18 hr. After cooling to room temperature, methanol was removed under reduced pressure. The residue was poured into 2 L of tert-butylmethyl ether with stirring and then the mixture was allowed to stand for 6 hr. The white precipitate was collected by filtered and was dried at 400 C under vacuum for 24 hr yielding 68 g of (3-chloropropyl)decylpiperidinium bromide as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06726905B1
Source datasetuspto-grants-2004_04
ORD IDord-ddc2d6ff010f4cbb8b4597140a977e67
Source noteuspto-grants-2004_04