HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 2-Trityloxycarbamoyl-benzo[b]thiophene-5-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(triphenylmethyl)hydroxylamine | HCID 3015602 | — |
| Reactant | 5-(Methoxycarbonyl)benzo[b]thiophene-2-carboxylic acid | HCID 59556409 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Trityloxycarbamoyl-benzo[b]thiophene-5-carboxylic acid methyl ester | HCID 86615044 | — |
Reaction Steps
A solution of benzo[b]thiophene-2,5-dicarboxylic acid 5-methyl ester (2.592 g, 10.97 mmol), O-trityl -hydroxylamine (3.020 g, 10.97 mmol), EDC (3.150 g, 16.48 mmol), HOBt (1.482 g, 10.97 mmol) and DIEA (4.80 mL, 27.6 mmol) in anhydrous THF (100 mL) was allowed to stir at rt for one week and then concentrated. To the residue was added MeOH (10 mL) and water (100 mL). The syrup obtained was washed with water (10 mL) and triturated with water (90 mL) to give 2-trityloxycarbamoyl-benzo[b]thiophene-5-carboxylic acid methyl ester as a pale solid. MS (EI): cal'd 243.1 (M-benzothiophene moiety+H+), exp 243.2 (M-benzothiophene moiety+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935724B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ca428f3e6b474114af183f0b7910d400 |
| Source note | uspto-grants-2011_05 |