Hydrochloric Acid → Dibenz(c,e)oxepin-5(7H)-one

HRID 1014074

반응식

HRID 1014074 반응식
[BH4-].[Na+].[C:3]12[C:10]3=[CH:11][CH:12]=[CH:13][CH:14]=[C:9]3[C:8](=O)[O:7][C:5](=[O:6])[C:4]1=[CH:16][CH:17]=[CH:18][CH:19]=2.Cl>CN(C=O)C.O>[CH:19]1[C:3]2[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[CH2:8][O:7][C:5](=[O:6])[C:4]=2[CH:16]=[CH:17][CH:18]=1

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 72794Diphenic anhydrideHCID 4311764Sodium borohydride

생성물 1

HCID 4613402Dibenz(c,e)oxepin-5(7H)-one수율 75.7%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

9.0 g (0.24 mol) of sodium borohydride were added in portions at 5° C. in the course of 10 min to a suspension of 50.0 g (0.22 mol) of diphenic anhydride in 220 ml of DMF. After stirring at RT for 1 h, the reaction mixture was poured onto 220 ml of 6 M hydrochloric acid, diluted with 750 ml of water and stirred for 2 h. The deposited precipitate was filtered off with suction and 35.0 g of 7H-dibenzo[c,e]oxepin-5-one were obtained; m.p. 131° C.

후처리

  1. stirringstirred for 2 h
  2. filtrationThe deposited precipitate was filtered off with suction

출처 및 근거

ORD 기록
ord-1785da442b1f474b9d269908dd09b37b
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07982045B2

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