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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156669Generated: October 31, 2026

HCID 54271791, compound → HCID 57253777, compound

https://huagongshe.com/reaction/1156669

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 numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-646bf0f07b2c4651a656c566cc7d42a4
Source noteuspto-grants-1982_06