HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698098Generated: October 31, 2026
Triisopropyl borate → tert-Butyl [5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)pyridin-2-yl]methylcarbamate
https://huagongshe.com/reaction/1698098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Neopentyl glycol | HCID 31344 | — |
| Reactant | tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamate | HCID 45789881 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl [5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)pyridin-2-yl]methylcarbamate | HCID 86626541 | — |
Reaction Steps
n-BuLi (27 mL, 2.5 M) was slowly added to a stirred solution of tert-butyl (5-bromopyridin-2-yl)methylcarbamate (17.7 g, 61.6 mmol) in THF (280 mL) at −78° C. under an argon atmosphere. After 5 min at −78° C., triisopropylborate (28.5 mL, 123 mmol) was added and the mixture was stirred at −78° C. for 1 h. Neopentyl glycol (6.4 g, 61.4 mmol) was added and the reaction mixture was allowed to reach rt and was stirred for 2.5 d. The reaction was quenched with water (300 mL). The phases were separated and the aqueous phase was extracted with DCM. The organic layer was concentrated and the residue was purified by two successive flash chromatographies (Heptane/EtOAc 9:1→1:4 and DCM/MeOH 24:1 respectively) to give the product (2.23 g) as a white solid. 1H NMR δ 8.57 (dd, 1H) 7.94 (dd, 1H) 7.65 (dd, 1H) 3.76 (s, 4H) 3.30 (s, 3H) 1.47 (s, 9H) 0.96 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163928B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d26c8a4f37e7411e99d8d605af81f8c3 |
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| Source note | uspto-grants-2012_04 |
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