Dimethyl Sulfoxide → HCID 15021998, 화합물

HRID 129268노트

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HRID 129268 반응식
CS(C)=O.C(Cl)(=O)C(Cl)=O.[OH:11][CH2:12][C:13]1([CH2:17][CH2:18][CH3:19])[CH2:16][O:15][CH2:14]1.C(N(CC)CC)C>ClCCl.O>[CH:12]([C:13]1([CH2:17][CH2:18][CH3:19])[CH2:16][O:15][CH2:14]1)=[O:11]

참가 물질

7

실험 절차

A solution of dimethyl sulphoxide (12 ml) in dry dichloromethane (4.0 ml) was added to a solution of oxalyl chloride (7.4 ml) in dichloromethane (25 ml) stirred at -70° under nitrogen. After the addition was complete the resulting mixture was stirred for a further 5 minutes at -70° before a solution of 3-hydroxymethyl-3-n-propyl oxetane (10.0 g) in dichloromethane (25 ml) was added, dropwise, over 10 minutes. The resulting mixture was allowed to stir for a further 30 minutes when neat triethylamine (54 ml) was added over approximately 30 minutes. The reaction mixture was allowed to warm to room temperature over 3 hours when it was poured into water. The organic phase was separated and the aqueous layer was further extracted with dichloromethane. The combined organic extracts were washed with dilute hydrochloric acid, saturated sodium bicarbonate and brine. The resulting organic phase was dried over anhydrous magnesium sulphate and evaporated in vacuo to give 3-formyl-3-n-propyloxetane (10.5 g) (European Patent Application No. 216624) as a yellow oil.

후처리

  1. additionAfter the addition
  2. additionwas added
  3. additionwas added over approximately 30 minutes
  4. customThe organic phase was separated
  5. extractionthe aqueous layer was further extracted with dichloromethane
  6. washThe combined organic extracts were washed with dilute hydrochloric acid, saturated sodium bicarbonate and brine
  7. dry with materialThe resulting organic phase was dried over anhydrous magnesium sulphate
  8. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-ca669fec1da746cfb610e5b050a4f3e1
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05466710

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