Hydrochloric Acid → HCID 178442823, 화합물

HRID 1112136노트

반응식

HRID 1112136 반응식
Cl[C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:13])[C:3]=1[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].[OH-:26].[Na+].Cl>C(O)C>[CH2:14]([C:3]1[C:4](=[O:13])[C:5]2[C:10]([C:11](=[O:12])[C:2]=1[OH:26])=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 1030502-Chloro-3-dodecyl-1,4-naphthoquinone

생성물 1

HCID 178442823HCID 178442823, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 10 parts of 3-chloro-2-n-dodecyl-1,4-naphthoquinone, 5 parts of 50% aqueous sodium hydroxide and 320 parts of 95% aqueous ethanol were heated at reflux for 15 minutes. The color of the mixture turned from yellow to dark red. The mixture was cooled to 25° and acidified with 10% aqueous hydrochloric acid. The color of the mixture was golden yellow after acidification. The product was filtered off and washed twice with water (25 parts) and twice with cold methanol (25 parts) to yield 8 parts of 2-n-dodecyl-3-hydroxy-1,4-naphthoquinone, mp. 85°-87° C.

후처리

  1. temperaturewere heated
  2. temperatureat reflux for 15 minutes
  3. temperatureThe mixture was cooled to 25°
  4. filtrationThe product was filtered off
  5. washwashed twice with water (25 parts) and twice with cold methanol (25 parts)

출처 및 근거

ORD 기록
ord-b09f234e260c40bf93b502016dc24170
출처 데이터셋
uspto-grants-1978_10
특허 번호
US04120897

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