HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839515Generated: October 25, 2026
Benzaldehyde → alpha-Cyanobenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate
https://huagongshe.com/reaction/839515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Cyclobutanone, 4-chloro-2,2,3,3-tetramethyl- | HCID 11105656 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-Cyanobenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate | HCID 14580510 | — |
Reaction Steps
A 50ml round-buttomed flask provided with a magnetic stirrer was charged with 10 mmol of benzaldehyde, 10 mmol of 2-chloro-3,3,4,4-tetramethylcyclobutanone, 12 mmol of sodium cyanide, 20 ml of a solvent and 1 ml of water. The reaction mixture was stirred vigorously at a temperature of 23° C. Two experiments ware carried out in this manner. Table II states the solvents used and presents the yields of the alpha-cyanobenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04096170 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-ad5b8ef185b843ffadb5fa0287118b04 |
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| Source note | uspto-grants-1978_06 |
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