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Sulfuryl chloride → 2-{3-[3-(4-n-Butoxyphenyl)-2-chloro-3-oxopropanamido]-4-chlorophenylcarboxy}ethyl-3,5-di-t-butyl-4-hydroxybenzoate

HRID 845370
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HRID 845370 반응식
S(Cl)([Cl:4])(=O)=O.[C:6]([C:10]1[CH:11]=[C:12]([CH:45]=[C:46]([C:49]([CH3:52])([CH3:51])[CH3:50])[C:47]=1[OH:48])[C:13]([O:15][CH2:16][CH2:17][C:18]([O:20][C:21]1[CH:26]=[CH:25][C:24]([Cl:27])=[C:23]([NH:28][C:29](=[O:44])[CH2:30][C:31]([C:33]2[CH:38]=[CH:37][C:36]([O:39][CH2:40][CH2:41][CH2:42][CH3:43])=[CH:35][CH:34]=2)=[O:32])[CH:22]=1)=[O:19])=[O:14])([CH3:9])([CH3:8])[CH3:7]>ClCCl>[CH2:40]([O:39][C:36]1[CH:35]=[CH:34][C:33]([C:31](=[O:32])[CH:30]([Cl:4])[C:29]([NH:28][C:23]2[CH:22]=[C:21]([O:20][C:18]([CH2:17][CH2:16][O:15][C:13](=[O:14])[C:12]3[CH:11]=[C:10]([C:6]([CH3:7])([CH3:8])[CH3:9])[C:47]([OH:48])=[C:46]([C:49]([CH3:51])([CH3:50])[CH3:52])[CH:45]=3)=[O:19])[CH:26]=[CH:25][C:24]=2[Cl:27])=[O:44])=[CH:38][CH:37]=1)[CH2:41][CH2:42][CH3:43]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 867422642-{3-[3-(4-n-Butoxyphenyl)-3-oxopropanamido]-4-chlorophenylcarboxy}ethyl 3,5-di-t-butyl-4-hydroxybenzoate

생성물 1

HCID 867422652-{3-[3-(4-n-Butoxyphenyl)-2-chloro-3-oxopropanamido]-4-chlorophenylcarboxy}ethyl-3,5-di-t-butyl-4-hydroxybenzoate수율 99%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Sulphuryl chloride (4.9 g, 36.2 mmole) in dichloromethane (10 ml) was slowly added to a solution of the 4 equivalent coupler from (f) (24.1 g, 36.2 mmole) in dichloromethane (140 ml). After stirring at room temperature for 21 hours, the volatiles were removed by rotary evaporation. The product was isolated as a yellow oil (25.1 g, 99%) and was used in the next reaction without further purification.

후처리

  1. customthe volatiles were removed by rotary evaporation

출처 및 근거

ORD 기록
ord-35cc148ce80d4261bee75b277fbf1728
출처 데이터셋
uspto-grants-1988_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04758501

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