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HCID 67042219, 화합물 → Methyl 4-amino-3,5-diisopropoxybenzoate

HRID 62749
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HRID 62749 반응식
[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([O:18][CH:19]([CH3:21])[CH3:20])[C:14]=1[N+:15]([O-])=O)[C:8]([O:10][CH3:11])=[O:9])([CH3:3])[CH3:2]>CO.C(O)=O.[Pd]>[NH2:15][C:14]1[C:13]([O:18][CH:19]([CH3:21])[CH3:20])=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][C:5]=1[O:4][CH:1]([CH3:3])[CH3:2]
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참가 물질

5

반응물 1

HCID 67042219HCID 67042219, 화합물

생성물 1

HCID 67041607Methyl 4-amino-3,5-diisopropoxybenzoate수율 74.4%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 284Formic Acid용매HCID 887Methanol용매

실험 절차

Methyl 3,5-diisopropoxy-4-nitrobenzoate (3) (594 mg, 2.00 mmol) was dissolved in a mixture of MeOH (40 mL) and formic acid (5 mL) and was passed through a Thales ‘H-cube’ cartridge (10% Pd/C) at a flow rate of 1 mL/min at 40° C. under H2 (full H2 mode). The solvents were removed in vacuo to yield methyl 4-amino-3,5-diisopropoxybenzoate (4) (398 mg, 72%) as a pale yellow oil: 1H NMR (400 MHz, CDCl3) δ: 7.20 (2H, s), 4.59 (2H, sep), 4.23 (2H, br s), 3.83 (3H, s), 1.33 (12H, d).

후처리

  1. customat 40° C.
  2. customThe solvents were removed in vacuo

출처 및 근거

ORD 기록
ord-91b05a97d1fd4cc3a351dc99a3c1c6c2
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447028B2

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