HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071306Generated: October 30, 2026
Ethyl bromoacetate → HCID 22393105, compound
https://huagongshe.com/reaction/1071306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 22393134 | HCID 22393134 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22393105 | HCID 22393105 | 99% |
Reaction Steps
Ethyl bromoacetate (0.13 ml), Na2CO3 (0.40 g) and tetrabutylammonium bromide (0.030 g) were added to a solution of 1,1-dioxo-3,3-dibutyl-5-phenyl-7-methoxy-8-hydroxy-2,3,4,5-tetrahydro-1,5-benzothiazepine (synthesised by the of WO9616051 for the corresponding 3-butyl-3-ethyl analogue; 0.400 g, 0.927 mmol) in MeCN (10 ml). The suspension was heated under reflux overnight before most of the solvent was removed under reduced pressure. The crude product was extracted (DCM/H2O) and filtered through a short silica-column (DCM:EtOAc-1:4) to give the title compound 0.476 g (99%). NMR (400 MHz 0.65-0.85 (m, 6H), 0.95-1.65 (m, 8H), 3.00-3.15 (m, 2H), 3.50-3.80 (m, 2H), 3.70-3.80 (s, 3H), 5.60 (s, 1H), 5.65 (d, 1H), 7.00-7.60 (m, 17H), 8.05-8.20 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06906058B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-a722e3e2ea544c948fedd51c81e6b591 |
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| Source note | uspto-grants-2005_06 |
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