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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701611Generated: October 30, 2026

Cyclohexanecarbonyl chloride → HCID 53644797, compound

https://huagongshe.com/reaction/1701611

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 numberUSRE030241
Source datasetuspto-grants-1980_03
ORD IDord-9db61f421ab44fd4a67974f88477ee75
Source noteuspto-grants-1980_03