HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746068Generated: November 1, 2026
Chlorotrimethylsilane → HCID 13359882, compound
https://huagongshe.com/reaction/746068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86740835 | HCID 86740835 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13359882 | HCID 13359882 | — |
Reaction Steps
To a solution of 4-phenylbutyl phosphonous acid, ethyl ester (0.5 g, 0.0022 mole) in chloroform (10 ml) was added triethylamine (0.34 ml, 0.0024 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (0.31 ml, 0.0024 mole) was added to the above solution dropwise, followed by ethyl bromoacetate (0.27 ml, 0.0024 mole). The ice bath was removed and the mixture stirred at room temperature for 6 hours and poured into 50% aqueous HCl (30 ml) and crushed ice (20 g). After shaking the mixture in a separatory funnel, the chloroform layer was separated and the aqueous layer extracted with dichloromethane (2×50 ml). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and the solvents removed on a rotavap. The resulting yellow oil (0.6 g) was vacuum dried to get 0.58 (84%) of title compound. TLC, silica gel, acetone:hexane (1:1), Rf =0.28.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04602092 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-d02b42002b4c4440a8821b76ee492632 |
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| Source note | uspto-grants-1986_07 |
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