6-Bromo-1-hexanol → 8-Bromooctyl prop-2-enoate

HRID 263831

반응식

HRID 263831 반응식
FC1C(F)=CC=CC=1C1C=C[C:12]([O:15]CCCCCCOC(=O)C=C)=[CH:11][CH:10]=1.[Br:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][OH:36].BrCCCCCCO>>[C:12]([O:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][Br:27])(=[O:15])[CH:11]=[CH2:10]

참가 물질

4

반응물 3

HCID 779706-Bromo-1-hexanolHCID 1626071-Octanol, 8-bromo-HCID 21459498HCID 21459498, 화합물

생성물 1

HCID 138413958-Bromooctyl prop-2-enoate수율 78%

실험 절차

The same procedure as in the synthesis (a) of Example 2 was repeated except that 34.7 g of 8-bromo-1-octanol were used instead of 30 g of 6-bromo-1-hexanol to give 34.1 g (Y., 78%) of 8-acryloyloxy-1-bromooctane. GC; 97%

출처 및 근거

ORD 기록
ord-9b95b3613e1d4bb6b5169caa15da0157
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05645760

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