HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749242Generated: October 31, 2026
(R)-2-Methyl-CBS-oxazaborolidine → 4-(Benzyloxy)-7-[(1R)-2-bromo-1-hydroxyethyl]-1,3-benzothiazol-2(3H)-one
https://huagongshe.com/reaction/749242
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-2-Methyl-CBS-oxazaborolidine | HCID 9838490 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | 4-(Benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-one | HCID 85939637 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Benzyloxy)-7-[(1R)-2-bromo-1-hydroxyethyl]-1,3-benzothiazol-2(3H)-one | HCID 68926570 | 69.8% |
Reaction Steps
A solution of [(R)-tetrahyro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo[1,2-c] [1,3,2]-oxazaborole] (22 μl of 1M in toluene) in dry THF(1 ml) was cooled to −5° C., stirring under nitrogen. Borane-methyl sulfide complex (2M solution in THF, 11 μl) was added and stirred for 10 min at −5° C. A solution of 4-(benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-one (47 mg) in dry THF (1.5 ml) was added dropwise and then another 66 μl of borane-methyl sulfide complex (2M solution in THF). The reaction mixture was left for 72 h at less than 5° C. and then partitioned between 2N HCl and ethyl acetate. The organic solution was dried (MgSO4), filtered and evaporated in vacuo. The residue was purified on a 5 g silica SPE cartridge, eluting with a stepped gradient of 10% to 25% ethyl acetate-cyclohexane mixtures to give the title compound (33 mg). LCMC RT=3.19 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402598B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-ce280e62366e4937bcc9a4de957cd692 |
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| Source note | uspto-grants-2008_07 |
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