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Hydrochloric Acid → rac-(2R,6S)-2,6-dimethylpiperidine-1-carbonyl chloride

HRID 2200018
ノート
印刷プレビュー

反応式

HRID 2200018 の反応式
[Cl:1][C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.N1C=CC=CC=1.[CH3:19][C@H:20]1[CH2:25][CH2:24][CH2:23][C@@H:22]([CH3:26])[NH:21]1.Cl>C(Cl)Cl>[CH3:19][C@H:20]1[CH2:25][CH2:24][CH2:23][C@@H:22]([CH3:26])[N:21]1[C:2]([Cl:1])=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 94429TriphosgeneHCID 641768rel-(2R,6S)-2,6-Dimethylpiperidine

生成物 1

HCID 94968704rac-(2R,6S)-2,6-dimethylpiperidine-1-carbonyl chloride収率 256.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
7.5 °C

実験手順

To a solution of triphosgene (20.8 g, 70.0 mmol) in DCM (400 mL) at 5° C. was added pyridine (16.2 mL, 200 mmol) dropwise over 10 min, maintaining the temperature below 10° C. The solution was then stirred between 5-10° C. for 1 h, then cis-2,6-dimethyl piperidine (CAS: 766-17-6, 27.0 mL, 200 mmol) was added dropwise over 10 min and the resulting red solution stirred at RT for 4 days (reaction complete within <4 h). The solution was cooled to 3° C., then a pre-cooled (3° C.) 1M aqueous HCl solution (400 mL) was added and the mixture stirred at 5° C. for 30 min. The mixture was separated and the aqueous layer was extracted with DCM (200 mL), then the combined organic extracts passed through a hydrophobic fit and concentrated under vacuum affording Intermediate 3a as a red oil (31.5 g, 90%). 1H NMR (300 MHz, CDCl3): 1.30 (6H, d, J=7.09 Hz), 1.49-1.87 (6H, m), 4.46-4.56 (2H, m).

後処理

  1. temperaturemaintaining the temperature below 10° C
  2. stirringthe resulting red solution stirred at RT for 4 days
  3. custom(reaction complete within <4 h)
  4. temperatureThe solution was cooled to 3° C.
  5. additionwas added
  6. stirringthe mixture stirred at 5° C. for 30 min
  7. customThe mixture was separated
  8. extractionthe aqueous layer was extracted with DCM (200 mL)
  9. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-31b6b74ed33945b5a154b2b2259c25c5
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09359354B2

反応ノート

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