HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576543Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 21511395, compound
https://huagongshe.com/reaction/1576543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | HCID 21511388 | HCID 21511388 | — |
| Product | HCID 21511395 | HCID 21511395 | 73.4% |
Reaction Steps
Into a 2 liter flask fitted with a 1 meter adiabatic column provided with a metallic lining, are placed: 400 g of 3-cyanomethyl-2-n-pentyl-1-cyclopentanone, 522 g of the glycoketal of methylethyl ketone and 4.5 g of paratoluenesulphonic acid. The mass is progressively heated in order to slowly distil the methyl ethyl ketone from the head of the column (temperature of the mass 128°-132°C; temperature of the vapour 80°C). The operation lasts about 5 hours. Then the excess glycoketal of methylethyl ketone is removed (temperature of the mass 132°-135°C; temperature of the vapour 110°-112°C). The mass is then cooled, 30 g of dry sodium carbonate added thereto, stirred for a half-hour and the mass washed to neutrality after diluting with 200 ml of ethyl ether. After distillation of the solvent and rectification of the crude product, there is obtained 360 g of 3-cyanomethyl-1,1-ethylenedioxy-2-n-pentyl-cyclopentane, which represents a yield of 73.4%. The product exhibits the following constants: b.p.0.5 = 136°-138°C, nD15 = 1.4724.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03981891 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-3e650417912243b6b9d6954f52b87343 |
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| Source note | uspto-grants-1976_09 |
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