홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Water → 3-Ethylbicyclo[3.2.0]hept-3-en-6-one

HRID 1500137
노트
인쇄 미리보기

반응식

HRID 1500137 반응식
[CH2:1]([CH:3]([CH2:9][CH:10]=[CH2:11])/[CH:4]=[CH:5]/[C:6]([OH:8])=O)[CH3:2].C(OC(=O)C)(=O)C.C(N(CC)CC)C.O>CN(C)C(=O)C>[CH2:1]([C:3]1[CH2:9][CH:10]2[CH:5]([CH:4]=1)[C:6](=[O:8])[CH2:11]2)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 12681390(2E)-4-Ethyl-2,6-heptadienoic acid

생성물 1

HCID 762854633-Ethylbicyclo[3.2.0]hept-3-en-6-one수율 81%

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매

반응 조건

온도
110 °C

실험 절차

(2E)-4-Ethylhepta-2,6-dienoic acid (34.0 g, purity: 90.7%) was dissolved in N,N-dimethylacetamide (100 mL) under the nitrogen atmosphere. To the solution, acetic anhydride (37.8 mL, 0.40 mol) and triethylamine (28 mL, 0.20 mol) were added. The reaction mixture was warmed and stirred at 105 to 115° C. for 6.5 hours. The reaction mixture was cooled to room temperature, and water (200 mL) was added thereto, followed by four extractions with n-hexane (150 mL×2 and 50 mL×2). All the extracted organic layers were combined and then washed with a saturated aqueous solution of sodium bicarbonate (50 mL) and water (50 mL) in this order. The obtained organic layer was concentrated under reduced pressure, and the residue was distilled under reduced pressure (93-102° C., approximately 25 mmHg) to obtain the title compound (22.06 g, colorless oil substance) (yield: 81%).

후처리

  1. temperatureThe reaction mixture was warmed
  2. temperatureThe reaction mixture was cooled to room temperature
  3. extractionfollowed by four extractions with n-hexane (150 mL×2 and 50 mL×2)
  4. washwashed with a saturated aqueous solution of sodium bicarbonate (50 mL) and water (50 mL) in this order
  5. concentrationThe obtained organic layer was concentrated under reduced pressure
  6. distillationthe residue was distilled under reduced pressure (93-102° C., approximately 25 mmHg)

출처 및 근거

ORD 기록
ord-813320f04b4442daab54809b85247511
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206104B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트