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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866705Generated: October 29, 2026

Acetic Anhydride → HCID 86735848, compound

https://huagongshe.com/reaction/866705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPropionic anhydrideHCID 31263—
ReactantHCID 21312669HCID 21312669—
ProductHCID 86735848HCID 86735848—

Reaction Steps

In the same manner but using the appropriate choice of compound of formula I (R1 =H) and lower alkanoic anhydride, then other compounds of formula I (R= lower alkanoyl and if R2 is CH2OR3 then R3 is lower alkanoyl) are prepared. For example the choice of trans-8-[2-(3-hydroxy-1-nonenyl)-3-isopropyl-5-oxocyclopentyl]octanoic acid (Example 144) and propionic anhydride instead of the compound of formula I and acetic anhydride noted in the procedure of this Example, give trans-8-[(2-(3-propionoxy-1-nonenyl)-3-isopropyl-5-oxocyclopentyl]octanoic acid. Similarly, ethyl trans-8-[2-3-hydroxy-1-heptenyl)-5-oxocyclopentyl]-6-octynoate (see Example 161) and butyric anhydride gives ethyl trans-8-[2-(3-butyryloxy-1-heptenyl)-5-oxocyclopentyl]-6-octynate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04100343
Source datasetuspto-grants-1978_07
ORD IDord-99be7c409d17486c85e142516e93e787
Source noteuspto-grants-1978_07