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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922634Generated: November 3, 2026

Triphenylphosphine → (1Z,3aR,4E,7aS)-4-(bromomethylene)-1-ethylidene-octahydro-7a-methyl-1H-indene

https://huagongshe.com/reaction/1922634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAzodicarboxylic acid dimethyl esterHCID 351621—
Reactant(R)-1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanolHCID 59456526—
SolventTetrahydrofuranHCID 8028—
Product(1Z,3aR,4E,7aS)-4-(bromomethylene)-1-ethylidene-octahydro-7a-methyl-1H-indeneHCID 5945652569.1%

Reaction Steps

Under a nitrogen atmosphere, a solution of (R)-1-{(E,3S,3aS,7aR)-7-(bromomethylene)-octahydro-3a-methyl-1H-indene-3-yl}ethanol (Compound 19: 20.8 mg, 0.07613 mmol) and triphenylphosphine (50 mg, 0.1903 mmol) in tetrahydrofuran (0.35 ml) was cooled in an ice bath, and azodicarboxylic acid dimethyl ester (2.7 M in toluene, 73.3 μl, 0.1979 mmol) was added dropwise thereto. The reaction mixture was stirred at the same temperature for 5 minutes and at room temperature for 40 hours, and then evaporated under reduced pressure. The obtained crude product was purified by flash column chromatography to obtain (1Z,3aR,4E,7aS)-4-(bromomethylene)-1-ethylidene-octahydro-7a-methyl-1H-indene (13.4 mg, 69.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173824B2
Source datasetuspto-grants-2012_05
ORD IDord-b0c4fecbdaeb4a3995a5975fc5b50914
Source noteuspto-grants-2012_05