HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458936Generated: October 29, 2026
Sodium Hydroxide → HCID 18442430, compound
https://huagongshe.com/reaction/458936
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18442431 | HCID 18442431 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18442430 | HCID 18442430 | 91.2% |
Reaction Steps
To a solution of 1,1-dioxo-3,3-dibutyl-5-(4-chlorophenyl)-7-methylthio-8-ethoxycarbonylmethoxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (Method 100; 0.195 g, 0.343 mmol) in ethanol (8 ml) was added NaOH (1.03 mmol in 0.5 ml water). The reaction mixture was stirred at room temperature for 70 min and then quenched by adding acetic acid (0.3 ml). The solvent was evaporated under reduced pressure and the residue was extracted with DCM/water. The organic layer was separated, washed with brine, dried and evaporated under reduced pressure to give the title compound 0.169 g (91%). NMR (500 MHz, CD3OD) 0.86 (t, 6H), 1.11–1.28 (m, 8H), 1.37–1.44 (m, 4H), 2.33 (s, 3H), 3.25 (s, 2H), 3.55 (s, 2H), 4.73 (s, 2H), 7.10–7.15 (m, 3H), 7.26 (s, 1H), 7.28–7.32 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192945B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-288cbbba2f134bd899bf4c363a07d3a0 |
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| Source note | uspto-grants-2007_03 |
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