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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390448Generated: October 30, 2026

HCID 21495456, compound → HCID 70552462, compound

https://huagongshe.com/reaction/1390448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21495456HCID 21495456—
ReactantHCID 70582738HCID 70582738—
ProductHCID 70552462HCID 70552462—

Reaction Steps

Following the procedure described above in Example 15A using alpha-methylcyclopropaneacetyl chloride instead of cyclohexanecarbonyl chloride the acylation product obtained is 3,4-bis(alpha-methylcyclopropaneacetoxy)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(alpha-methylcyclopropaneacetoxy)-alpha-(tert-butylaminomethyl)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138581
Source datasetuspto-grants-1979_02
ORD IDord-9b18296b4d8f41a18b7d3088d3e61539
Source noteuspto-grants-1979_02