2,2-Bis(trifluoromethyl)decanoyl fluoride → Sodium 2,2-bis(trifluoromethyl)decanoate

HRID 3951

反応式

HRID 3951 の反応式
[F:1][C:2]([F:20])([F:19])[C:3]([C:15]([F:18])([F:17])[F:16])([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[C:4](F)=[O:5].C[Si](C)(C)[O-:23].[Na+:26]>CCOCC>[F:1][C:2]([F:20])([F:19])[C:3]([C:15]([F:18])([F:17])[F:16])([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[C:4]([O-:23])=[O:5].[Na+:26]

参加物

4

反応物 2

HCID 201535092,2-Bis(trifluoromethyl)decanoyl fluorideHCID 23672319Sodium trimethylsilanolate

生成物 1

HCID 23684024Sodium 2,2-bis(trifluoromethyl)decanoate

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

The procedure of Example 1 was followed using 2,2-bis(trifluoromethyl)decanoyl fluoride (6.11 g, 19.7 mmol), sodium trimethylsilanolate (2.21 g, 19.7 mmol) and dry ether (20 mL). The product, sodium 2,2-bis(trifluoromethyl)decanoate, was isolated as a waxy solid (5.5 g, 85% yield) by concentrating the filtrate under vacuum: 1H NMR (CDCl3) δ 0.88 (m, CH3, 3H), 1.30 (m, CH2, 12H), 2.10 ppm (m, CH2, 2H); 19F NMR (D2O/acetone) δ -62.0 ppm (brs, CF3,6F). Anal. Calcd. for C12H17F6NaO2 : C, 43.64; H, 5.19; F, 34.52. Found: C, 44.34; H, 5.10; F, 35.58.

出典と根拠

ORDレコード
ord-9f0abb4433aa4985acae6632fd7a6977
出典データセット
uspto-grants-1988_02
特許番号
US04723016

関連ノート

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