作者:H. Goldwhite、M.S. Gibson、C. Harris
DOI:10.1016/s0040-4020(01)99163-x
日期:1964.1
Chlorocarbonylmethanesulphonyl chloride reacts with hept-1-ene in the presence of benzoyl peroxide to give γ-chlorononanoyl chloride in 30–40% yield. The homogeneity and structure of this product follow from conversion to (a) a single amide, and (b) the known γ-nonanolactone and derived hydrazide respectively.
氯羰基甲烷磺酰氯在过氧化苯甲酰的存在下与庚-1-烯反应,以30-40%的收率得到γ-氯壬酰氯。该产物的均质性和结构来自分别转化为(a)单一酰胺和(b)已知的γ-壬内酯和衍生的酰肼。