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Benzyl Bromide → HCID 86690094, 화합물

HRID 520377
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인쇄 미리보기

반응식

HRID 520377 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[O:9]=[C:10]1[CH2:19][C:12]2([CH2:15][CH:14]([C:16]([OH:18])=[O:17])[CH2:13]2)[CH2:11]1.CCN(C(C)C)C(C)C>C(Cl)(Cl)Cl.C(#N)C>[O:9]=[C:10]1[CH2:11][C:12]2([CH2:15][CH:14]([C:16]([O:18][CH2:2][C:3]3[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=3)=[O:17])[CH2:13]2)[CH2:19]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7498Benzyl BromideHCID 81531DiisopropylethylamineHCID 336952306-Oxospiro[3.3]heptane-2-carboxylic acid

생성물 1

HCID 86690094HCID 86690094, 화합물

시약·촉매·용매 2

HCID 6212Chloroform용매2회HCID 6342Acetonitrile용매

실험 절차

A solution of (bromomethyl)benzene (564 mg) in CHCl3 (1 mL) was added to a stirred solution of 6-oxospiro[3.3]heptane-2-carboxylic acid (462 mg) and DIPEA (0.576 mL) in acetonitrile (2 mL) and CHCl3 (2 mL) and the mixture was stirred at rt overnight. The reaction mixture was evaporated to dryness and then purified by silica gel FCC (1:1 DCM:hexanes) to afford benzyl 6-oxospiro[3.3]heptane-2-carboxylate as a clear oil.

후처리

  1. customThe reaction mixture was evaporated to dryness
  2. custompurified by silica gel FCC (1:1 DCM:hexanes)

출처 및 근거

ORD 기록
ord-6ba32ce6867541d787fcc22a433c322f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09326973B2

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