HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756439Generated: October 27, 2026
Chlorotrimethylsilane → HCID 21474481, compound
https://huagongshe.com/reaction/1756439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Iodobenzoic acid | HCID 12085 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 21474481 | HCID 21474481 | — |
Reaction Steps
11.4 g (0.170 mol) of powdered zinc and 50 ml of THF are-introduced into a three-necked flask, 2.2 ml of trimethylsilyl chloride are added and the mixture is stirred for 15 minutes, 28 ml (0.174 mol) of tert-butyl 2-bromoacetate are then introduced dropwise and the mixture is stirred for 30 minutes. It is cooled to 0° C. (icebath), 5 g (4.3 mmol) of tetrakis(triphenylphosphine)palladium(0), 10.8 g (43.5 mmol) of 4-iodobenzoic acid and 50 ml of HMPA are introduced and the mixture is heated to 40° C. for one hour. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (95:5). After evaporation of the solvents, 8.1 g (80% ) of the expected product, melting point 132°-133° C., are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05439925 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-bee08751d21849c8a1879da26a27c4c3 |
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| Source note | uspto-grants-1995_08 |
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