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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1,2-Cyclopropanedicarboxylic acid, trans-

HRID 1768448
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HRID 1768448 반응식
C([O:3][C:4]([C@@H:6]1[CH2:8][C@H:7]1[C:9]([O:11]CC)=[O:10])=[O:5])C.Cl.[Na+].[Cl-]>[OH-].[Na+]>[C@@H:7]1([C:9]([OH:11])=[O:10])[CH2:8][C@H:6]1[C:4]([OH:5])=[O:3]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 117153031,2-Diethyl (1R,2R)-1,2-cyclopropanedicarboxylate

생성물 1

HCID 69504501,2-Cyclopropanedicarboxylic acid, trans-

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

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온도
22 °C

실험 절차

Diethyl carboxylate 3 (16.9 g, 19.3 mmol) was dissolved in 170 ml of 2N NaOH and heated under reflux for 1 h. The solution was stirred for additional 18 h at 22° C. The solution was cooled, adjusted to pH 3 with 2N HCl, saturated with NaCl, and finally extracted with ethyl acetate (2×100 ml). The pooled extracts were dried (Na2SO4), evaporated to dryness, and the white residue was used for the next step without further purification (8.5 g, 79%); mp 175–176° C. 1H-NMR (D2O): δ 1.42 (m, 2H), 2.18 (m, 4H).

후처리

  1. temperatureheated
  2. temperatureunder reflux for 1 h
  3. temperatureThe solution was cooled
  4. extractionfinally extracted with ethyl acetate (2×100 ml)
  5. dry with materialThe pooled extracts were dried (Na2SO4)
  6. customevaporated to dryness
  7. customthe white residue was used for the next step without further purification (8.5 g, 79%)

출처 및 근거

ORD 기록
ord-eafa451b143c4798beed215005a9e1bc
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07235695B2

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