HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447390Generated: October 30, 2026
Triethylamine → (E)-4-((4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)thiazol-2-yl)methyl) morpholine
https://huagongshe.com/reaction/447390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5233012 | — |
| Reactant | 4-((4-Bromothiazol-2-yl)methyl)morpholine | HCID 66723338 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-4-((4-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)thiazol-2-yl)methyl) morpholine | HCID 66734172 | — |
Reaction Steps
To a solution of 4-((4-bromothiazol-2-yl)methyl)morpholine (125 mg, 0.5 mmol) and triethylamine (0.2 mL, 1.5 mmol) in DMF (1.5 mL) was added 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxaborolane (0.15 mL, 1 mmol) and Pd(Ptert-Bu3)2 (8 mg, 0.002 mmol). The mixture was heated to 120° C. under microwave irradiation for 1 h. Ethyl acetate (50 mL) was added and the solution was washed with water (2×10 mL) and brine (10 mL), dried over MgSO4 and concentrated to an orange oil (165 mg, 99%). 1H NMR (400 MHz, CDCl3) δ 7.31 (d, J=18.0 Hz, 1H), 7.19 (s, 1H), 6.40 (d, J=18.0 Hz, 1H), 3.84 (s, 2H), 3.74 (bs, 4H), 2.61 (bs, 4H), 1.29 (s, 12H); MS ESI 337.1 [M+H]+, calcd for [C16H25BN2O3S+H]+ 337.2. [α]22.8°D=169° (c 0.42, Methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481533B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-569a4fae19ea4a11bcff484b5742171e |
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| Source note | uspto-grants-2013_07 |
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