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Hydrochloric Acid → 6-(9-oxoacridin-10(9H)-yl)hexanoic acid

HRID 1171809
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HRID 1171809 반응식
[O:1]=[C:2]1[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N:9]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][C:21]([O:23]CC)=[O:22])[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.Cl>C(O)(=O)C>[O:1]=[C:2]1[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N:9]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][C:21]([OH:23])=[O:22])[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 59554584HCID 59554584, 화합물

생성물 1

HCID 101931936-(9-oxoacridin-10(9H)-yl)hexanoic acid수율 49.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
100 °C

실험 절차

To ethyl 6-(9-oxoacridin-10(9H)-yl)hexanoate (0.80 g) was added acetic acid (9 ml) and 2M hydrochloric acid (2.5 ml). The mixture was heated to 100° C. for 18 hours after which time the volatile components were removed on a rotary evaporator. Diethyl ether was added (25 ml) and the mixture stirred for 15 minutes. The resulting material was filtered off and air dried to give 0.36 g final product (Formula XVII). Mass spectrum: 310 (M+H).

후처리

  1. customwere removed on a rotary evaporator
  2. additionDiethyl ether was added (25 ml)
  3. filtrationThe resulting material was filtered off
  4. customair dried

출처 및 근거

ORD 기록
ord-144ca0faa4ec4f8ea091f513922ed966
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829714B2

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