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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684503Generated: October 31, 2026

1-Bromoeicosane → HCID 15340538, compound

https://huagongshe.com/reaction/1684503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromoeicosaneHCID 20271—
Reactant2H-Pyran, tetrahydro-2-(10-undecyn-1-yloxy)-HCID 103566—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 15340538HCID 1534053861.6%

Reaction Steps

5 g (0.0198 mol) of 11-tetrahydropyranyloxyundecyne of Example 7 were placed in a mixture of 50 ml of THF and 25 ml of hexamethylphosphoric triamide under an argon atmosphere. At -60° C., 12.4 ml (0.0198 mol) of n-butyllithium in hexane were added dropwise. After 30 min at -60° C., a solution of 9.0 g (0.0248 mol) of 1-bromoeicosane in 25 ml of THF was added dropwise at -60° C. The mixture was left to warm up to room temperature. After 18 h at room temperature, it was poured into 25% aqueous NaH2PO4 solution and extracted with n-heptane (3×). The combined organic phases were dried (Na2SO4) and the solvent was removed. Flash chromatography on silica gel (n-heptane/ethyl acetate =15:1) gave 6.5 g (61.3% of theory) of 1-tetrahydropyranyloxy-hentriacont-10-yne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641767
Source datasetuspto-grants-1997_06
ORD IDord-0fab22d819784f878b6e2afc57c65faa
Source noteuspto-grants-1997_06