HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159396Generated: October 26, 2026
Water → 1-(3-{[Tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzyl)pyrrolidine
https://huagongshe.com/reaction/1159396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-{[Tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzaldehyde | HCID 13861697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-{[Tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzyl)pyrrolidine | HCID 68619343 | 94% |
Reaction Steps
Pyrrolidine (6.8 mL, 82 mmol) was added to a solution of intermediate 32, 3-{[tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzaldehyde (16.7 g, 66 mmol) in dichloromethane (200 mL). The reaction mixture was cooled on ice bath, and sodium triacetoxyborohydride (17.4 g, 82 mmol) was added in portions under stirring. The reaction mixture was intensively stirred for 12 h at RT. Water (100 mL) was added. The organic layer was separated. The aqueous one was extracted with CH2Cl2 (2×100 mL). The organic layer was washed with brine, dried over Na2SO4 and evaporated in vacuo to give the title compound (19 g, 94%, 60 mmol). 1H NMR data (DMSO-d6): 6.92-7.03 (m, 2H, H—Ar), 6.83-6.91 (m, 1H, H—Ar), 3.58 (d, 2H, J=1.7 Hz, Ar—CH2); 2.38-2.46 (m, 4H), 1.63-1.70 (m, 4H) 0.97 (s, 9H, t-Bu), 0.16 (s, 6H, 2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812040B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-23325a5608b54831bf46bf1f947513ed |
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| Source note | uspto-grants-2010_10 |
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