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Hydrochloric Acid → (3-(2-Fluorobenzyl)piperidin-3-yl)methanol

HRID 530881
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반응식

HRID 530881 반응식
Cl.[F:2][C:3]1[CH:24]=[CH:23][CH:22]=[CH:21][C:4]=1[CH2:5][C:6]1([CH2:19][OH:20])[CH2:11][CH2:10][CH2:9][N:8](C(OC(C)(C)C)=O)[CH2:7]1>O1CCOCC1>[F:2][C:3]1[CH:24]=[CH:23][CH:22]=[CH:21][C:4]=1[CH2:5][C:6]1([CH2:19][OH:20])[CH2:11][CH2:10][CH2:9][NH:8][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 67983173HCID 67983173, 화합물

생성물 1

HCID 56754765(3-(2-Fluorobenzyl)piperidin-3-yl)methanol

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

Hydrochloric acid in dioxane (1.5 mL, 4M) was added to a flask containing tert-butyl 3-(2-fluorobenzyl)-3-(hydroxymethyl)piperidine-1-carboxylate (0.43 g, 1.33 mmol). 1,4-dioxane (1.5 mL) was added to the reaction mixture. The reaction was allowed to stir for 4 hours. Upon reaction completion, the reaction was concentrated, and 346 mg of crude product was recovered and progressed to the next step without further purification.

후처리

  1. customUpon reaction completion
  2. concentrationthe reaction was concentrated
  3. custom346 mg of crude product was recovered
  4. customprogressed to the next step without further purification

출처 및 근거

ORD 기록
ord-d8fc6c7eb35a4955a9e29ca0a3a4ecf1
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09351965B2

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