Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701620Generated: November 1, 2026

HCID 54271791, compound → HCID 57253777, compound

https://huagongshe.com/reaction/1701620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54271791HCID 54271791—
ReactantHCID 56980747HCID 56980747—
ProductHCID 57253777HCID 57253777—

Reaction Steps

Following the procedure described above in Example 15A but using cycloheptanepropionyl chloride instead of cyclohexanecarbonyl chloride the acylation product obtained is 3,4-bis(cycloheptanepropionyloxy)phenyl tert-butylaminomethyl ketone; and when this product is catalytically hydrogenated, using the procedure described above in Example 15B, there is obtained 3,4-bis(cycloheptanepropionyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030241
Source datasetuspto-grants-1980_03
ORD IDord-881d3969e9c94774874763b44d224c7f
Source noteuspto-grants-1980_03