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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156685Generated: October 25, 2026

Phenoxyacetyl chloride → HCID 53690513, compound

https://huagongshe.com/reaction/1156685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenoxyacetyl chlorideHCID 69703—
ReactantIsoproterenone hydrochlorideHCID 2830496—
ProductHCID 53690513HCID 53690513—

Reaction Steps

Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and phenoxyacetyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(phenoxyacetoxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(phenoxyacetoxy)-alpha-(isopropylaminomethyl)benzyl alcohol methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-8d10ca0cf045458aac95ffa20d37d498
Source noteuspto-grants-1982_06