SU157979A1 - - Google Patents
Info
- Publication number
- SU157979A1 SU157979A1 SU781584A SU781584A SU157979A1 SU 157979 A1 SU157979 A1 SU 157979A1 SU 781584 A SU781584 A SU 781584A SU 781584 A SU781584 A SU 781584A SU 157979 A1 SU157979 A1 SU 157979A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- compounds
- alcohols
- dihydrofuran
- acetates
- mol
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- -1 hydroxycarbamyl compounds Chemical class 0.000 description 4
- JKTCBAGSMQIFNL-UHFFFAOYSA-N 2,3-dihydrofuran Chemical compound C1CC=CO1 JKTCBAGSMQIFNL-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU157979A1 true SU157979A1 (cs) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69711391T2 (de) | Verbessertes verfahren zum herstellen von geschützten 3,4-dihydroxybuttersäure estern | |
| TW499426B (en) | Process for the production of five-membered or six-membered cyclic ethers, and anhydropolyol compositions obtained thereby | |
| RU2056414C1 (ru) | СПОСОБ ПОЛУЧЕНИЯ СОЛИ ЦИС- β -ФЕНИЛГЛИЦИДИЛОВОЙ-(2R,3R) КИСЛОТЫ | |
| US20180319759A1 (en) | A process for preparing a mixture comprising 5-(hydroxymethyl) furfural and specific hmf esters | |
| CN103781754B (zh) | 制备饱和烷基酯/酸的方法 | |
| SU157979A1 (cs) | ||
| US5350868A (en) | ω-hydroxy-(ω-3)-ketonitrile and method for preparing ω-hydroxyaliphatic acid | |
| WO2013005749A1 (ja) | テトラヒドロフランの製造方法 | |
| Hillers et al. | Ozonolysis of cyclic enol ethers: an efficient strategy to aldol and homoaldol compounds | |
| US2372654A (en) | Manufacture of substances promoting the growth of yeast and other unicellular plants | |
| JP5949227B2 (ja) | テトラヒドロフランの製造方法 | |
| Swadesh et al. | Mechanism of hydrogenation of 2-methylfuran | |
| SU484680A3 (ru) | Способ получени сложного метилового эфира (3-кето-2-пропилцикло-пентил)-уксусной кислоты | |
| EP0219199B1 (en) | Method for preparation of lactones | |
| SU159505A1 (cs) | ||
| RU2319690C1 (ru) | Способ получения эфиров левулиновой кислоты | |
| SK280170B6 (sk) | Spôsob výroby alkylesterov tetronovej kyseliny | |
| WO2013005747A1 (ja) | 1,4-ブタンジオール含有組成物 | |
| JP3098825B2 (ja) | ジヒドロフラノン誘導体の製造方法 | |
| JP5915409B2 (ja) | 1,4−ブタンジオールの製造方法 | |
| SU248700A1 (ru) | Способ получения бисфульвенов фуранового | |
| WO2001094329A1 (de) | Verfahren zur herstellung von 2-coumaron und substituierten 2-coumaronen | |
| SU192801A1 (cs) | ||
| RU731721C (ru) | 5-(1-адамантил)-2-пирролидон, обладающий психотропной активностью, и способ его получения | |
| SU274119A1 (ru) | Способ получения 7-оксипроизводных тионафтена |