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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156679Generated: October 31, 2026

Phenolate Sodium → HCID 54364113, compound

https://huagongshe.com/reaction/1156679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolate SodiumHCID 4445035—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 14696615HCID 14696615—
ReactantHCID 20535365HCID 20535365—
ProductHCID 54364113HCID 54364113—

Reaction Steps

Following a procedure similar to that described in Example 30A above, when 3-hydroxy-4-(7,7-dimethyloctanoyloxy)-phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is reacted with p-isopropoxyphenylacetyl chloride there is obtained 3-(p-isopropoxyphenylacetoxy)-4-(7,7-dimethyloctanoyloxy)phenyl tert-butylaminomethyl ketone which reacts with methanesulfonic acid to yield the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using the procedure described above in Example 30B, there is obtained 3-(p-isopropoxyphenylacetoxy)-4-(7,7-dimethyloctanoyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-c9ddcbdba78b4955892a121b1b2a7ab9
Source noteuspto-grants-1982_06