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Sevoflurane → 1,1,3,3,3-Pentafluoro-2-(fluoromethoxy)-1-propene

HRID 530181
ノート
印刷プレビュー

反応式

HRID 530181 の反応式
[CH2:1]([F:12])[O:2][CH:3]([C:8](F)([F:10])[F:9])[C:4]([F:7])([F:6])[F:5].C(OCOCC)C>>[F:5][C:4]([F:6])([F:7])[C:3]([O:2][CH2:1][F:12])=[C:8]([F:9])[F:10]
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 2

HCID 5206SevofluraneHCID 10024Diethoxymethane

生成物 1

HCID 1050151,1,3,3,3-Pentafluoro-2-(fluoromethoxy)-1-propene

実験手順

30 grams of sevoflurane (0.15 mols) was cooled to about −36.2° C. under nitrogen. Approximately 10 mL of a 3.0 M solution of CH3Li/CH2(OC2H5)2 (0.03 mols of the base) was added over 29 minutes while maintaining a temperature between about −37.5° C. and about −30.5° C. After addition of the methyl lithium was complete, the addition funnel was washed with a few mL of diethoxymethane. The reaction mixture was then stirred for approximately 20 minutes at a temperature between about −39° C. and about −35° C. A vacuum (0.3 mmHg) applied to the reaction mixture for approximately 1 hour, 46 minutes while the reaction mixture was held at a temperature between about −38.5° C. and about 10.7° C. afforded approximately 30.0 grams of a crude liquid product. GC analysis of this liquid showed it contained 22.8% compound A, 47.1% unreacted sevoflurane, and 29.7% diethoxymethane.

出典と根拠

ORDレコード
ord-d7180bfd1f1d41e285eb71f3b18d58b5
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09353038B2

反応ノート

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