Organic Syntheses 2003
DOI: 10.1002/0471264180.os076.22
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6‐Chloro‐1‐Hexene and 8‐Chloro‐1‐Octene

Abstract: 6‐chloro‐1‐hexene and 8‐chloro‐1‐octene intermediate: Allylmagnesium bromide reactant: allyl bromide (181.60 g, 1.50 mol) product: 6‐Chloro‐1‐hexene reactant: 1‐bromo‐3‐chloropropane (150.00 g, 0.95 mol) reactant: 1‐bromo‐5‐chloropentane (88.37 g, 0.47 mol) … Show more

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Cited by 2 publications
(1 citation statement)
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“…At this point, we elongated the side chain of compound 8 with allylmagnesium bromide [ 15 ] ( Scheme 6 ) obtaining compound 9 in 52% yield. The product seems to be homogenous either by TLC and column chromatography, however the 13 C-NMR spectrum shows duplicates for seven out of the expected 14 signals, suggesting the formation of two diastereoisomers.…”
Section: Resultsmentioning
confidence: 99%
“…At this point, we elongated the side chain of compound 8 with allylmagnesium bromide [ 15 ] ( Scheme 6 ) obtaining compound 9 in 52% yield. The product seems to be homogenous either by TLC and column chromatography, however the 13 C-NMR spectrum shows duplicates for seven out of the expected 14 signals, suggesting the formation of two diastereoisomers.…”
Section: Resultsmentioning
confidence: 99%