HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710346Generated: October 29, 2026
Formaldehyde → tert-Butyl 5-(4-(3-((4-fluorophenyl)(methyl)amino)propyl)phenethyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate
https://huagongshe.com/reaction/710346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl-5-(4-(3-(4-fluorophenylamino)propyl)phenethyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 131733946 | — |
| Catalyst | 1,2-Dichloroethane | HCID 11 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 5-(4-(3-((4-fluorophenyl)(methyl)amino)propyl)phenethyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 131733947 | — |
Reaction Steps
To a stirred solution of the product of Step C (0.04 g, 0.08 mmol), formaldehyde solution in H2O (0.25 ml) in 1,2-dichloroethane (5 ml) 4 drops of DIPEA was added at room temperature, followed by 5 drops of AcOH and NaBH(OAc)3 (0.04 g, 0.19 mmol). The mixture was stirred overnight at room temperature and diluted to 20 ml with CH2Cl2. The organic layer was washed with aqueous NaHCO3, H2O, dried over MgSO4 and filtered. The filtrate was evaporated to dryness and the residue was purified by FCC (SiO2) to give the product (0.035 g), as creamy paste. 1H-NMR (CDCl3) 1.40 (s, 3H); 1.42 (s, 3H); 1.46 (s, 9H); 1.84-1.99 (m, 4H); 2.5-2.61 (m, 4H); 2.85 (s, 3H); 3.25 (tr, 2H, J=7.41 Hz); 3.66 (d, 2H, J=11.8 Hz); 3.88 (d, 2H, J=11.7 Hz); 4.85 (s, 1H); 6.54-6.59 (m, 2H); 6.86-6.92 (m, 2H); 7.07 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181182B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-cbbf0595e4e148e4bfd2d6a0d6f7165c |
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| Source note | uspto-grants-2015_11 |
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