HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652015Generated: October 28, 2026
Chloride → 14-(Trimethylsilyl)tetradecanoic acid
https://huagongshe.com/reaction/652015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | 11-Bromoundecanoic acid | HCID 17812 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromopropyltrimethylsilane | HCID 12845800 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178504203 | HCID 178504203 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 14-(Trimethylsilyl)tetradecanoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670421 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-38895bee317b4e67b81ad1f60d153b19 |
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| Source note | uspto-grants-1987_06 |
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