HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109695Generated: November 3, 2026
Sodium borohydride → HCID 178444482, compound
https://huagongshe.com/reaction/1109695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl cyano-[4-(1E-pentenyl)cyclohexylidene]acetate | HCID 19019238 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178444482 | HCID 178444482 | 20% |
Reaction Steps
A solution of 46.0 g of ethyl cyano-[4-(1E-pentenyl)cyclohexylidene]acetate in 120 ml of ethanol is added dropwise at 5°-10° C. within 40 minutes to a mixture of 6.7 g of sodium borohydride and 120 ml of ethanol. The reaction mixture is stirred at 5° C. for 45 minutes, then diluted with 750 ml of water and extracted with three 250 ml portions of diethyl ether. The extract is washed neutral with water, dried over sodium sulphate and concentrated. There is obtained crude ethyl cyano-[trans-4-(1E-pentenyl)cyclohexyl]acetate (cis content <20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05322638 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-cbbe6e6ddc504fa3aac856bb6bd8c708 |
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| Source note | uspto-grants-1994_06 |
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