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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638571Generated: November 1, 2026

Triphenylphosphine → HCID 56611422, compound

https://huagongshe.com/reaction/1638571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 56630262HCID 56630262—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 56611422HCID 56611422—

Reaction Steps

A stirred solution of the γ-lactone of (2S,4S,5S)-4,5-dihydroxy-2-isopropyl-7-methyloctanoic acid from Preparation IIIA (0.214 g., 1 mmol) and triphenylphosphine (0.289 g., 1.1 mmol) in benzene (3 ml) is cooled in an ice bath and treated during 5-10 minutes with N-bromosuccinimide (0.196 g., 1.1 mmol). The mixture is kept cold for an additional 30 minutes and then at ambient temperature for 4 hours. It is diluted with Et2O and filtered. The filtrate is con-centrated and the residue chromatographed on silica gel (100 g.) with 7.5% EtOAc-hexane. The product, the γ-lactone of (2S,4S,5R)-5-bromo-4-hydroxy-2-isopropyl-7-methyloctanoic acid, thus obtained was crystallized from cold pentane to give 0.061 g., m.p. 62.5°-63.5° C. and 0.054 g., m.p. 60°-62.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880781
Source datasetuspto-grants-1989_11
ORD IDord-5af084ea27434330b43d07866a44cfd0
Source noteuspto-grants-1989_11