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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031509Generated: November 2, 2026

tert-Butyl acrylate → HCID 19989926, compound

https://huagongshe.com/reaction/1031509

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantAcrylateHCID 25188—
ReactantBenzeneacetonitrile, 4-bromo-HCID 27914—
ReactantSodium borohydrideHCID 4311764—
CatalystPalladiumHCID 23938—
CatalystCobalt(II) chlorideHCID 24288—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 19989926HCID 19989926—

Reaction Steps

p-Bromophenylacetonitrile is first condensed with t-butyl acrylate under conditions of the palladium acetate catalyzed Heck reaction. The resulting acrylate is hydrogenated with palladium on charcoal catalyst followed by reduction (of the cyano group) with sodium borohydride in the presence of cobalt(II) chloride to yield t-butyl p-(2-aminoethyl)-phenylpropionate. Condensation with 2-alpha,3-alpha-dihydroxy-4β-[9-(2-chloroadenyl)]-cyclopentane-1β-N-ethylcarboxamide yields the t-butyl ester of compound (a) which is hydrolyzed to compound (a) with aqueous hydrochloric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954504
Source datasetuspto-grants-1990_09
ORD IDord-ae5f9b9bd9984ba48be9de154ea5bfd0
Source noteuspto-grants-1990_09