HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33699Generated: October 26, 2026
Acetic Acid → Ammonia methanol dichloromethane
https://huagongshe.com/reaction/33699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-piperazine hydrochloride | HCID 9924012 | — |
| Product | 1-Isopropyl-4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-piperazine | HCID 9928168 | — |
| Product | Ammonia methanol dichloromethane | HCID 21584172 | 5% |
Reaction Steps
A solution of the product of Example 25 (122 mg), acetone (23 mg), and acetic acid (19 mg) in dichloroethane (3 mL) was treated with sodium triacetoxyborohydride (96 mg). After 14 h, the reaction was quenched with saturated aqueous sodium bicarbonate, and the aqueous phase was extracted with dichloromethane (120 mL). The organic phase was dried (magnesium sulfate) and evaporated in vacuo. Silica gel chromatography of the residue (5% 2M ammonia-methanol/dichloromethane) gave the title compound as a white solid (31 mg). 1H NMR (400 MHz, CDCl3): 6.91-6.87 (m, 2H), 6.85-6.81 (m, 2H), 3.95 (t, J=6.4 Hz, 2H), 3.10 (t, J=4.9 Hz, 4H), 2.69 (t, J=4.9 Hz, 4H), 2.48-2.44 (m, 2H), 2.39 (bs, 4H), 1.98-1.91 (m, 2H), 1.61-1.56 (m, 4H), 1.46-1.40 (m, 2H), 1.09 (d, J=6.5 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429586B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-2eb1d2c5976f4473b28a36104e19f9c8 |
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| Source note | uspto-grants-2008_09 |
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