HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267786Generated: October 31, 2026
Potassium Cyanide → HCID 21553920, compound
https://huagongshe.com/reaction/267786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 21553945 | HCID 21553945 | — |
| Reactant | HCID 21553969 | HCID 21553969 | — |
| Product | HCID 21553920 | HCID 21553920 | — |
Reaction Steps
The 3-amino-4-cyano-6-benzyloxy-3,4-dihydro-2H-1,5-benzodioxepin and/or its 9-benzyloxy isomer is converted to 3-oxo-6-benzyloxy-3,4-dihydro-2H-1,5-benzodioxepin by the procedure described in Example 1, Step C, and the 3-keto compound then reacted with potassium cyanide by either the process of Step D of Example 1 or the alternative procedure there described to provide 3-hydroxy-3-cyano-6-benzyloxy-3,4-dihydro-2H-1,5-benzodioxepin. This product then is reduced with lithium aluminum hydride by the method outlined in the alternate of Step E, Example 1, to give 3-hydroxy-3-aminomethyl-6-benzyloxy-3,4-dihydro-2H-1,5-benzodioxepin which when reacted with acetone and then reduced by the process of Step F, Example 1, there is obtained 3,6-dihydroxy-3-isopropylaminomethyl-3,4-dihydro-2H-1,5-benzodioxepin hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03944560 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-3b6cc185a6fe448b9211184e5cad41fc |
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| Source note | uspto-grants-1976_03 |
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