Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390438Generated: November 2, 2026

Cyclohexanecarbonyl chloride → HCID 53644797, compound

https://huagongshe.com/reaction/1390438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantCycloheptanecarbonyl chlorideHCID 12556870—
ReactantHCID 20535439HCID 20535439—
ProductHCID 53644797HCID 53644797—

Reaction Steps

When cycloheptanecarbonyl chloride is substituted for the cyclohexanecarbonyl chloride in the procedure described in Example 15A above, the acylation product obtained is 3,4-bis(cycloheptanecarbonyloxy)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(cycloheptanecarbonyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138581
Source datasetuspto-grants-1979_02
ORD IDord-4642a0e8f8a14c9e84a9d053fa26d161
Source noteuspto-grants-1979_02