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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390447Generated: October 30, 2026

HCID 54271791, compound → HCID 57253777, compound

https://huagongshe.com/reaction/1390447

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 numberUS04138581
Source datasetuspto-grants-1979_02
ORD IDord-d9f3befd670e41c3a891fe41b909ceea
Source noteuspto-grants-1979_02