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HCID 178471800, 화합물 → HCID 178471796, 화합물

HRID 409497
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HRID 409497 반응식
[CH2:1]([O:3][C:4]([CH2:6][C@H:7]1[CH2:12][CH2:11][C@H:10]([C:13](O)=[O:14])[CH2:9][CH2:8]1)=[O:5])[CH3:2]>C1COCC1>[CH2:1]([O:3][C:4](=[O:5])[CH2:6][C@H:7]1[CH2:12][CH2:11][C@H:10]([CH2:13][OH:14])[CH2:9][CH2:8]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178471800HCID 178471800, 화합물

생성물 1

HCID 178471796HCID 178471796, 화합물수율 83%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of trans-4-ethoxycarbonylmethyl-cyclohexanecarboxylic acid (1 mmol; 214 mg) in THF (3 mL) is added 1.0 M THF solution of borane THF complex (2 mmol; 2 mL) at 0° C. under nitrogen. The solution is stirred for 1.5 hours at room temperature, quenched by dropwise addition of 1 mL of MeOH. The mixture after concentration is diluted with dichloromethane and saturated aqueous ammonium chloride solution. The product is extracted with 100 ml of dichloromethane. The organic layer after dried is separated, concentrated under reduced pressure. The residue is purified by column chromatography on silica gel (n-hexane/EtOAc) to give trans-(4-hydroxymethylcyclohexyl)-acetic acid ethyl ester (166 mg, 83%); ESI-MS m/z: 201 [M++1], Retention time 1.67 min (condition A).

후처리

  1. customquenched by dropwise addition of 1 mL of MeOH
  2. concentrationThe mixture after concentration
  3. additionis diluted with dichloromethane and saturated aqueous ammonium chloride solution
  4. extractionThe product is extracted with 100 ml of dichloromethane
  5. customThe organic layer after dried
  6. customis separated
  7. concentrationconcentrated under reduced pressure
  8. customThe residue is purified by column chromatography on silica gel (n-hexane/EtOAc)

출처 및 근거

ORD 기록
ord-5acc975b83c547b993ffd23a44d9cd4e
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759365B2

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