http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11349585-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c8d4dc7bd1a30d8fda907fceaeb4e69 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D327-10 |
| filingDate | 1998-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b241e44e1b875fe18eed90e478adc81f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e3c42f02d7d9549f3901dfb2e96ee83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a69f08ff1177c33a263a93d7f8db5a15 |
| publicationDate | 1999-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H11349585-A |
| titleOfInvention | Method for producing 2-oxo-1,3-dioxa-2-thiolane derivative |
| abstract | (57) [Problem] To provide an industrially useful production route of a 2-oxo-1,3-dioxa-2-thiolane derivative. SOLUTION: The following general formula (1): (Wherein, R represents a hydrocarbon group which may have a substituent). In producing a 2-oxo-1,3-dioxa-2-thiolane derivative represented by the following formula (2): Embedded image 1,2,3,4-butanetetraol represented by the following general formula (3) in which only a primary hydroxyl group is sulfonylated by reacting with a sulfonylating agent in a solvent in the presence of a base in a solvent. Embedded image 1,4-di-O-organosulfonyl-1,2,3,4-butanetetraol represented by the following formula, followed by reacting a thionylating agent to form a thiolane skeleton A method for producing a 2-oxo-1,3-dioxa-2-thiolane derivative. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100832128-B1 |
| priorityDate | 1998-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 53.