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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Hydrochloric Acid → HCID 13543373、化合物

HRID 1048857
ノート
印刷プレビュー

反応式

HRID 1048857 の反応式
[CH2:1]([N:8]1[C:13](=[O:14])[CH2:12][O:11][CH2:10][CH:9]1[C:15](O)=[O:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[BH4-].[Na+].Cl>C1COCC1.C(OC(Cl)=O)C.O>[CH2:1]([N:8]1[CH:9]([CH2:15][OH:16])[CH2:10][O:11][CH2:12][C:13]1=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 4311764Sodium borohydrideHCID 135433704-Benzyl-5-oxomorpholine-3-carboxylic acid

生成物 1

HCID 13543373HCID 13543373、化合物収率 40.2%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒
HCID 10928Ethyl chloroformate溶媒

実験手順

To a stirred solution of 4-benzyl-5-oxomorpholine-3-carboxylic acid (450 mg, 1.91 mmole) and triethylamine (0.28 mL, 2.5 mmole) in THF, ethylchloroformate (0.2 mL) was added dropwise for 20 min at −10° C. The reaction mixture was stirred for additional 30 min and filtered. The filtrate was added for 30 min to a solution of NaBH4 (200 mg, 5.28 mmole) in water (15 mL) at 0° C. The reaction mixture was stirred for 4 h at 10° C. and acidified with 2M HCl. THF was evaporated under reduced pressure and the aqueous residue extracted into DCM, washed with saturated NaHCO3 (20 mL), dried over Na2SO4, concentrated and purified by flash chromatography using eluent 5% MeOH in DCM to get the title compound (170 mg) as oily mass, m/z 222.

後処理

  1. filtrationfiltered
  2. stirringThe reaction mixture was stirred for 4 h at 10° C.
  3. customTHF was evaporated under reduced pressure
  4. extractionthe aqueous residue extracted into DCM
  5. washwashed with saturated NaHCO3 (20 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. custompurified by flash chromatography

出典と根拠

ORDレコード
ord-8e8dce59fd514ec19db799e091855e4a
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09382216B2

反応ノート

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