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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702964Generated: October 26, 2026

Acetyl chloride → Succinate

https://huagongshe.com/reaction/1702964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSuccinyl chlorideHCID 10970—
ReactantPentanedioyl dichlorideHCID 17887—
ReactantBruceolideHCID 99531—
ReactantMethyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylateHCID 12302104—
ProductSuccinateHCID 160419—
ProductGlutarate(2-)HCID 4418048—
Product3,5-Dioxohexanoic acidHCID 5459844—

Reaction Steps

In accordance with the above procedure, but where, in place of 3,4-dimethyl-2-pentenoyl chloride, there is utilized benzoyl chloride, trimethoxybenzoyl chloride or cinnamoyl chloride there is obtained the corresponding 3-ester or 3,15-diester. Similarly, but where, in place of bruceolide, there is utilized brusatol and as an acid chloride there is utilized succinoyl chloride, glutaroyl chloride and acetyl chloride, there is obtained 3,3-bisbrusatolyl succinate, 3,3-bisbrusatolyl glutarate and 3,11,12-brusatolyl triacetate, 3, 11, 12 bis brusatolyl triacetate can also be prepared by acetylation with pyridine in acetic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350638
Source datasetuspto-grants-1982_09
ORD IDord-233cfa63431c469c810679ed744ad36f
Source noteuspto-grants-1982_09