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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390437Generated: November 2, 2026

Cyclohexanecarbonyl chloride → HCID 54083988, compound

https://huagongshe.com/reaction/1390437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantCyclopentanecarbonyl chlorideHCID 78284—
ReactantHCID 20535454HCID 20535454—
ProductHCID 54083988HCID 54083988—

Reaction Steps

When cyclopentanecarbonyl chloride is substituted for the cyclohexanecarbonyl chloride in the procedure described in Example 15A above, the acylation product obtained is 3,4-bis(cyclopentanecarbonyloxy)phenyl tert-butylaminomethyl ketone; and when this product is catalytically hydrogenated using the procedure described in Example 15B above, there is obtained 3,4-bis(cyclopentanecarbonyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138581
Source datasetuspto-grants-1979_02
ORD IDord-9ee07819a8c9455cbe208cd68a3daa1a
Source noteuspto-grants-1979_02