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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566441Generated: October 30, 2026

Triphenylphosphine → HCID 178459243, compound

https://huagongshe.com/reaction/566441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 178459253HCID 178459253—
SolventBenzeneHCID 241—
ProductHCID 178459243HCID 178459243124.3%

Reaction Steps

A mixture of 1.994 grams (11.57 mmol) of trans-p-menthane-7,8diol (for preparation, see: Ohloff, G.; Giersch, W. Helv. Chim. Acta., 1980, 63, 76), 3.035 grams (11.57 mmol) of triphenylphosphine, and 20 mL of benzene was chilled in an ice bath and treated portionwise with 2.060 grams (11.57 mmol) of N-bromosuccinimide. The ice bath was removed and the mixture was stirred for 16 hours at room temperature. The mixture was diluted with 50 mL of hexane and the solids were removed by filtering sequentially through celite and filter paper. The filtrate was washed with 0.5 Na2S2O3 solution (2×100 mL), 1 N sodium hydroxide solution (1×50 mL), brine (1×50 mL), dried (Na2SO4), and evaporated. The residue was diluted with hexane and filtered to remove triphenylphospineoxide. The residue was purified by flash chromatography using a 10-50% EtOAc-hexane eluant to give 3.382 grams (88%) of the title compound an oil. 1H NMR (CDCl3) d 0.93-1.28 (6H, m), 1.15 (6H, s), 1.58 (1H, br s), 1.83-2.00 (4H, m), 3.27 (2H, d, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174895B1
Source datasetuspto-grants-2001_01
ORD IDord-c537a9ed5f8544579f8a6585b4584a36
Source noteuspto-grants-2001_01