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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652015Generated: October 28, 2026

Chloride → 14-(Trimethylsilyl)tetradecanoic acid

https://huagongshe.com/reaction/652015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant11-Bromoundecanoic acidHCID 17812—
ReactantLithium ChlorideHCID 433294—
ReactantMagnesiumHCID 5462224—
Reactant3-BromopropyltrimethylsilaneHCID 12845800—
ReactantHCID 178418573HCID 178418573—
ReactantHCID 178504203HCID 178504203—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product14-(Trimethylsilyl)tetradecanoic acidHCID 13884857—

Reaction Steps

A solution of 240 g. 11-bromoundecanoic acid in 1.15 l. dry tetrahydrofuran was cooled to -20° under nitrogen, and to this stirred solution was dropwise added 309 ml. of a 3M solution of methyl magnesium bromide in ether followed by a solution of 1.54 g. lithium chloride and 2.43 g. cuprus chloride in 90 ml. dry tetrahydrofuran. The mixture was stirred at -20° while a warm solution of 3-(trimethylsilyl)propyl magnesium bromide, prepared from 266 g. 3-(trimethylsilyl)propyl bromide and 33.7 g. magnesium turnings in 860 ml. dry tetrahydrofuran, was added dropwise. The reaction was stirred at -20° for 30 min. after addition was complete, then at room temperature for 18 hr. The mixture was poured into 4 l. toluene and washed twice with 4 l. of 10% sulfuric acid and once with 4 l. 1N hydrochloric acid containing 375 ml. methanol. Evaporation of the toluene and distillation at reduced pressure yielded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670421
Source datasetuspto-grants-1987_06
ORD IDord-38895bee317b4e67b81ad1f60d153b19
Source noteuspto-grants-1987_06