JPS56147780A - 3-allyl-5-hydroxymethyltetrahydrofuran-2-ones - Google Patents
3-allyl-5-hydroxymethyltetrahydrofuran-2-onesInfo
- Publication number
- JPS56147780A JPS56147780A JP5074380A JP5074380A JPS56147780A JP S56147780 A JPS56147780 A JP S56147780A JP 5074380 A JP5074380 A JP 5074380A JP 5074380 A JP5074380 A JP 5074380A JP S56147780 A JPS56147780 A JP S56147780A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- hydroxymethyltetrahydrofuran
- allyl
- compound shown
- give
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Furan Compounds (AREA)
Abstract
NEW MATERIAL:3-Allyl-5- hydroxymethyltetrahydrofuran-2- ones shown by the formula I (R1 and R2 are H or 1W4C alkyl; R3 is H or OH-protecting group).
EXAMPLE: (3R, 5S)-3-Allyl-3-ethyl-5-hydroxymethyltetrahydrofuran-2-one.
USE: A raw material for a nontryptamine part of the precursor of a physiologically active indolealkaloid(hypotensive, cerebrovascular vasodilator, antitumor agent). The raw material is industrially advantageous.
PROCESS: For example, 5-hydroxymethyltetrahydrofuran-2-one shown by the formula II obtained from glutamic acid is reacted with a compound shown by the formula R'3X (R' is OH-protecting group; X is halogen), to give a compound shown by the formula III, which is reacted with an ally halide in the presence of a base, e.g., lithium isopropylamide to give a compound shown by the formula IV. This compound is alkylated with an alkyl halide, to give a compound shown by the formula I wherein R3 is R3'.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5074380A JPS56147780A (en) | 1980-04-17 | 1980-04-17 | 3-allyl-5-hydroxymethyltetrahydrofuran-2-ones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5074380A JPS56147780A (en) | 1980-04-17 | 1980-04-17 | 3-allyl-5-hydroxymethyltetrahydrofuran-2-ones |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56147780A true JPS56147780A (en) | 1981-11-16 |
JPH0115510B2 JPH0115510B2 (en) | 1989-03-17 |
Family
ID=12867313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5074380A Granted JPS56147780A (en) | 1980-04-17 | 1980-04-17 | 3-allyl-5-hydroxymethyltetrahydrofuran-2-ones |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56147780A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56150078A (en) * | 1979-12-22 | 1981-11-20 | Dynamit Nobel Ag | Substituted lactone, its manufacture and pentanecarboxylic acid derivative |
-
1980
- 1980-04-17 JP JP5074380A patent/JPS56147780A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56150078A (en) * | 1979-12-22 | 1981-11-20 | Dynamit Nobel Ag | Substituted lactone, its manufacture and pentanecarboxylic acid derivative |
Also Published As
Publication number | Publication date |
---|---|
JPH0115510B2 (en) | 1989-03-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES8400407A1 (en) | 2(1H)-pyridinones and preparation thereof. | |
MY101618A (en) | Intermediates for the production of epipodophyloxin and related compounds and processes for the preparation and use thereof | |
ES8506569A1 (en) | Substituted indonaphthols used in detecting ions. | |
JPS56147780A (en) | 3-allyl-5-hydroxymethyltetrahydrofuran-2-ones | |
JPS5731671A (en) | Preparation of homopiperazine derivative | |
ES8506586A1 (en) | Meta- and para-isopropenyl-alpha,alpha-dimethylbenzylamine. | |
ES8206542A1 (en) | Process for the preparation of phosphonoformaldehyde-hydrate. | |
AU568101B2 (en) | Pharmaceutical benzazepines and benzdiazepines | |
MY105374A (en) | A process for the preparation of 7-amino-3-methoxymeth- yl-ceph-3-em-4-carboxylic acid. | |
JPS579754A (en) | Preparation of methylene dicarbanilate | |
SU1147711A1 (en) | Method of obtaining 6-aryl-2-thiouracils | |
JPS56142285A (en) | Esterifying method of penicillin | |
JPS5461153A (en) | Inositolsulfate ammonium salt and its preparation | |
JPS6442449A (en) | Production of p-phenoxyphenol | |
JPS56138176A (en) | Preparation of thiolcarbamate derivative | |
JPS57156469A (en) | Preparation of tetrazole derivative | |
ES8600760A1 (en) | +/- 2-((3,4-Methylenedioxy)phenethyl)-5-((3-carboxamido-4-hydroxy)-alpha-hydroxybenzyl)pyrrolidines, pharmaceutical compositions containing them, process for their production and intermediates therefor. | |
JPS56123976A (en) | Novel preparation of optically active 2,3-epoxyaldehyde derivative | |
JPS56147781A (en) | 3-allyl-5-hydroxytetrahydrofuran-2-ones | |
ES8305721A1 (en) | Process and intermediates for preparing pirbuterol and analogs. | |
JPS55141472A (en) | Synthesis of 1,4-disubstituted-1,2-dihydroquianzolin-2-one | |
IE831445L (en) | Process for the production of 1-ethoxycarbonyloxyethyl ester¹of 6-(d-(-)-ó-amino-ó-phenylacetamido) penicillanic acid | |
ES2003299A6 (en) | Process for the preparation of condensed as-triazine derivatives | |
JPS5589284A (en) | Preparation of xanthine derivative | |
JPS5242813A (en) | Synthetic process for dihydrolavandulal |