HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024332Generated: October 28, 2026
2-Nitrobenzoyl chloride → HCID 86718834, compound
https://huagongshe.com/reaction/1024332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| Reactant | Bis(trimethylsilyl)acetylene | HCID 84564 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86718834 | HCID 86718834 | 99.1% |
Reaction Steps
A solution of 2-nitrobenzoyl chloride (13) (225 g; 1.2 moles) and 1,2-bis(trimethylsilyl)ethyne (205 g; 1.2 moles) in dichloromethane (3 L) was cooled to 0° C. Aluminum chloride (159.2 gram, 1.2 moles) was slowly added at 0° C. over 10 minutes while keeping the internal reaction temperature below 10° C. After the addition, the reaction mixture was stirred at 5-10° C. for 1 hour. With stirring, the black reaction mixture was poured into ice-water mixture (2 kg of ice and 1 kg of water). The resulting suspension was filtered and the filter cake was washed with dichloromethane (200 mL). The organic phase of the combined filtrate was separated. The aqueous phase was extracted 2-times with dichloromethane (2×2 L). The combined organic phase was washed with water (2 L), filtered through a Celite pad (200 g), dried over sodium sulfate (120 g), and concentrated at the temperature below 30° C. (bath temperature) to dryness to give 294 g (99% yield) of the desired product in 95% HPLC purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722886B1 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-5e1c2017966e49c1a7fc42e025be4b63 |
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| Source note | uspto-grants-2014_05 |
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