Acetyl chloride → HCID 178477169, 화합물

HRID 1824614

반응식

HRID 1824614 반응식
C[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[S:7])=[CH:4][CH:3]=1.[C:10](Cl)(=[O:12])[CH3:11]>>[C:10]([SH:7]=[CH:6][C:5]1[CH:4]=[CH:3][CH:2]=[CH:9][CH:8]=1)(=[O:12])[CH3:11]

참가 물질

3

반응물 2

HCID 6367Acetyl chlorideHCID 181775354-Methylthiobenzaldehyde

생성물 1

HCID 178477169HCID 178477169, 화합물

실험 절차

Two other S-protected p-thiobenzaldehydes were obtained as shown in Scheme 2 (FIG. 15). The thiocyanato-benzaldehyde 8 was prepared according to a general procedure (Suzuki and Abe (1996) Synth. Commun., 26: 3413–3419) in 20% yield. All attempts to improve the yield by replacement of DMF with 1,3-dimethyl-2-imidazolidinone, increasing the temperature, or prolonging the reaction time were unsuccessful. S-Acetylthiobenzaldehyde 9 was prepared in a two-step one-flask procedure. Cleavage of the methyl group of 4-methylthiobenzaldehyde according to a general procedure (Tiecco et al. (1982) Synthesis, 478–480) followed by trapping of the resulting anion with acetyl chloride afforded the desired S-acetylthiobenzaldehyde 9 in 55% yield.

후처리

  1. temperatureincreasing the temperature
  2. customS-Acetylthiobenzaldehyde 9 was prepared in a two-step one-flask procedure

출처 및 근거

ORD 기록
ord-d7077d35dd3e40f2bb3eff350e30453b
출처 데이터셋
uspto-grants-2006_05
특허 번호
US07042755B1

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