HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866705Generated: October 29, 2026
Acetic Anhydride → HCID 86735848, compound
https://huagongshe.com/reaction/866705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | HCID 21312669 | HCID 21312669 | — |
| Product | HCID 86735848 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04100343 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-99be7c409d17486c85e142516e93e787 |
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| Source note | uspto-grants-1978_07 |
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