Methane → 3-Phenyl-2-propen-1-yl acetate

반응식

C(O[C:9]([C:11]1[CH:16]=[CH:15][C:14](COC(=O)C)=[CH:13][CH:12]=1)=[CH2:10])C1C=CC=CC=1.C(OC(C1C=CC=C([CH2:38][O:39][C:40](=[O:42])[CH3:41])C=1)=C)C1C=CC=CC=1.ClCC=CC1C=CC=CC=1.C>>[C:40]([O:39][CH2:38][CH:10]=[CH:9][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)(=[O:42])[CH3:41]

참가 물질

반응물 4

HCID 297Methane

HCID 94242Benzene, (3-chloro-1-propenyl)-

HCID 21253608alpha-Benzyloxy[4-(acetoxymethyl)styrene]

HCID 21253611alpha-Benzyloxy[3-(acetoxymethyl)styrene]2회

생성물 1

HCID 76603-Phenyl-2-propen-1-yl acetate

실험 절차

α-Benzyloxy[4-(acetoxymethyl)styrene] and α-Benzyloxy[3-(acetoxymethyl)styrene] (Formula II, R1 =CH3COOCH2C6H4 -, R2 =benzyl). (Acetoxymethyl)styrene was prepared from (chloromethyl)styrene by the method described in Polymer, 1973, 14, 330. It was converted (Method C) to the required alkoxystyrene: 1H NMR (CCl4) δ 2.02 (3H, s), 4.23 (1H, d, J 2 Hz), 4.67 (1H, d, J 2 Hz), 4.87 (2H, s), 5.00 (2H, s), 7.0-7.7 (9H, m); MS (CH4) 283 (MH+, 1%), 91 (100%); IR 1740 cm-1.