Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (5-(3-Thienyl)tetrazol-1-yl)acetic acid | HCID 3035658 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54030218 | HCID 54030218 | 60.3% |
Reaction Steps
To a solution of 1 g (4.76 mM) of [5-(3-thienyl)tetrazol-1-yl] acetic acid and 514 mg (5.71 mM) of 1,4-butanediol in 10 ml of N,N-dimethylformamide was added 1.08 g (5.23 mM) of dicyclohexylcarbodiimide at room temperature. After the mixture was stirred at room temperature for 30 min, a small amount of acetic acid was added to the mixture and then was stirred for 30 min. The mixture was poured into ice-water. The precipitated crystal was filtered off and washed with water. The filtrate was extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography (eluent: chloroform/ethyl alcohol=30/1) for separation and purification, to give 810 mg (yield 60.3%) of [5-(3-thienyl)tetrazol-1-yl] acetic acid 4-hydroxybutyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05262433 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-041007bf1efb4c338981c4f54b04519a |
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| Source note | uspto-grants-1993_11 |
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