HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987316Generated: October 29, 2026
4-tert-Butylbenzoyl chloride → HCID 69629012, compound
https://huagongshe.com/reaction/987316
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylbenzoyl chloride | HCID 74372 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86595065 | HCID 86595065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69629012 | HCID 69629012 | 89% |
Reaction Steps
3-{4-[2-(4-Aminophenyl)ethoxy]phenyl}-(S)-2-ethoxypropanoic acid hydro chloride (described in Example 56a) (0.2 g; 0.547 mmole) was dissolved in tetrahydrofurane (5 ml). Sodium hydrogencarbonate (0.053 g; 0.631 mmole) was added and the mixture was stirred for a little while. 4-tert-Butylbenzoyl chloride (0.118 g; 0.6 mmole) was added. The reaction mixture was stirred overnight and then evaporated to dryness. Dichloromethane and water were added to the residue and the phases were separated. The organic phase was dried with magnesium sulfate and the solvent was evaporated. Chromatography of the residue on silica gel (Isolute, SI) using dichloromethane:heptane (1:1), dichloromethane and finally methanol:dichloromethane (1:99) as eluants gave 0.238 g (89% yield) of 3-{4-[2-{4-(4-[tert-butyl]benzoyl)aminophenyl}ethoxy]phenyl}-2-(S)-ethoxypropanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630600B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-9e0ca8fcd0bf46d091d7354787f756ff |
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| Source note | uspto-grants-2003_10 |
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