反应 #4021417
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1cdc69081b8b4fd3b06f941c4104cc00暂无可渲染的结构数据
C(CCCCCCCO)CCCCCCCO产品信息
1,15-十五烷二醇(CAS 14722-40-8)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1cdc69081b8b4fd3b06f941c4104cc00反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-745e13b4ea504b77ae2db9f1d72e3d50反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Lithium aluminium hydride (1.52 g, 40.0 mmol, 2.0 eq.) was suspended in dry THF (80 mL) under an argon atmosphere. A solution of 15-pentadecanolide (4.80 g, 20.0 mmol) in dry THF (200 mL) was added at 0° C. Stirring was continued at this temperature for 1 h and for 3 more hours at r.t. Potassium sodium tartrate solution (20%, 50 mL) was added dropwise to the stirred reaction mixture. The phases were separated and the aqueous phase was extracted with diethyl ether (3×100 ml). The combined organic layers were dried over MgSO4. The solvent was removed in vacuo and the product was isolated as a white solid, which was used for the next step without purification. Yield: 4.68 g (96%). The phases were separated the aqueous phase was extracted with diethyl ether (3×100 ml) The combined organic layers were dried over MgSO4 The solvent was removed in vacuo the product was isolated as a white solid, which was used for the next step without purification
来源 ID: ord-d5db7491e832471b9c8214e13eeda5d5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1cdc69081b8b4fd3b06f941c4104cc00反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-745e13b4ea504b77ae2db9f1d72e3d50反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A 54 g portion of the hydrogenated product obtained in Reference Example 2 and 0.2 g of magnesium oxide were put into the same apparatus of Inventive Example 1 and the reaction was carried out under conditions of 230 to 260° C. and 1.3 kPa to 130 Pa to obtain 15.2 g of a colorless liquid distillate 3 hours thereafter. This distillate contained 2.2 g of cyclopentadecanolide (yield 94%), 0.93 g of 1,15-pentadecanediol (recovery ratio 96%) and 11.3 g of 2-decyl-1-tetradecanol. The reaction residue was a light yellow liquid having a viscosity of 85 mPa·s, and 28.4 g of di-2-decyl-1-tetradecyl pentadecandioate was recovered from the residue (recovery ratio 85%).
来源 ID: ord-6e08d86a544d4eca84f606ea63371f18反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Lithium aluminium hydride (1.52 g, 40.0 mmol, 2.0 eq.) was suspended in dry THF (80 mL) under an argon atmosphere. A solution of 15-pentadecanolide (4.80 g, 20.0 mmol) in dry THF (200 mL) was added at 0° C. Stirring was continued at this temperature for 1 h and for 3 more hours at r.t. Potassium sodium tartrate solution (20%, 50 mL) was added dropwise to the stirred reaction mixture. The phases were separated and the aqueous phase was extracted with diethyl ether (3×100 ml). The combined organic layers were dried over MgSO4. The solvent was removed in vacuo and the product was isolated as a white solid, which was used for the next step without purification. Yield: 4.68 g (96%). The phases were separated the aqueous phase was extracted with diethyl ether (3×100 ml) The combined organic layers were dried over MgSO4 The solvent was removed in vacuo the product was isolated as a white solid, which was used for the next step without purification
来源 ID: ord-d5db7491e832471b9c8214e13eeda5d5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1cdc69081b8b4fd3b06f941c4104cc00PubChem References
以下资料来自该化合物的公开数据库参考记录。
