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1-Bromo-4-(trimethoxymethyl)benzene → HCID 20075599, 화합물

HRID 704132
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HRID 704132 반응식
[OH:1][CH2:2][C:3]([CH2:8][OH:9])([CH2:6][CH3:7])[CH2:4][SH:5].CO[C:12](OC)(OC)[C:13]1[CH:18]=[CH:17][C:16]([Br:19])=[CH:15][CH:14]=1>C(N(CC)CC)C>[Br:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]23[S:5][CH2:4][C:3]([CH2:6][CH3:7])([CH2:8][O:9]2)[CH2:2][O:1]3)=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 135812791-Bromo-4-(trimethoxymethyl)benzeneHCID 21217019HCID 21217019, 화합물

생성물 1

HCID 20075599HCID 20075599, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

(iv)a) 2,2-Di-(hydroxymethyl)-butanethiol (0.5 g.), trimethyl 4-bromo-orthobenzoate 2 (1.0 g.) and triethylamine (0.1 ml.) were heated at 130°, under a current of nitrogen, for 45 minutes. The volatile components were removed in vacuo (2.00 mm.), at 140°. The residue was purified by chromatography on alumina (alumina Woelm TSC) eluting with 1:6 dichloromethane: hexane, saturated with ammonia. 1-(4-Bromophenyl)-4-ethyl-2,6-dioxa-7-thiabicyclo[2,2,2]octane was obtained as colourless crystals (80 mg.).

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  1. customThe volatile components were removed in vacuo (2.00 mm.), at 140°
  2. customThe residue was purified by chromatography on alumina (alumina Woelm TSC)
  3. washeluting with 1:6 dichloromethane

출처 및 근거

ORD 기록
ord-c436bd95336e4c189ce3e98cb329d2e6
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985582

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