101376-26-5

基本信息
(R)-4-芐基-嗎啉-3-甲醇
(R)-4-芐基-3-羥甲基嗎啉
(R)-(4-芐基嗎啉-3-基)甲醇
(R)-(4-芐基-3-嗎啡啉)-甲醇
(3R)-4-(苯基甲基)-3-嗎啉甲醇
R-4-芐基-3-羥甲基嗎啉/(R)-(4-芐基-3-嗎啡啉)-甲醇
(R)-(4-BenzylMorpholin-3-yl)Methanol
[(3R)-4-benzylMorpholin-3-yl]Methanol
(R)-4-BENZYL-3-HYDROXYMETHYLMORPHOLINE
(R)-4-Benzyl-3-hydroxymethyloorpholine
(R)-4-Benzly-3-hydroxymethylmorpholine
(R)-4-(phenylmethyl)-3-Morpholinemethanol
(3R)-4-(Phenylmethyl)-3-morpholinemethanol
3-Morpholinemethanol, 4-(phenylmethyl)-, (3R)-
物理化學(xué)性質(zhì)
制備方法

106973-37-9

101376-26-5
以(S)-4-芐基-5-氧代-3-嗎啉甲酸為原料合成(R)-(4-芐基-3-嗎啡啉)-甲醇的一般步驟:向中間體66((S)-4-芐基-5-氧代-3-嗎啉甲酸,12.6g,53.6mmol)的四氫呋喃(200mL)溶液中緩慢加入硼烷-四氫呋喃絡(luò)合物(1.0M,348mL)。反應(yīng)混合物在室溫下攪拌6小時后,加入甲醇淬滅反應(yīng),隨后加熱至80℃并繼續(xù)攪拌2小時。反應(yīng)完成后,向混合物中加入飽和碳酸氫鈉水溶液和乙酸乙酯進行萃取。水層用乙酸乙酯再次萃取,合并有機層。有機層依次用水和鹽水洗滌,經(jīng)無水硫酸鈉干燥后,減壓濃縮除去溶劑。所得粗產(chǎn)物通過硅膠柱層析(洗脫劑:己烷/乙酸乙酯=90/10至10/90梯度洗脫)純化,得到目標產(chǎn)物(R)-(4-芐基-3-嗎啡啉)-甲醇(9.60g,46.0mmol,收率86%)。質(zhì)譜(ESI+)顯示分子離子峰m/z 208([M+H]+,100%)。
參考文獻:
[1] Patent: WO2011/111875, 2011, A1. Location in patent: Page/Page column 90-91
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985, p. 2577 - 2580
[3] Helvetica Chimica Acta, 2004, vol. 87, # 1, p. 90 - 105