HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16605Generated: October 30, 2026
Hydrochloric Acid → HCID 86602123, compound
https://huagongshe.com/reaction/16605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 86602122 | HCID 86602122 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86602123 | HCID 86602123 | 67% |
Reaction Steps
To a stirred mixture of 2-benzyl-α,α-dimethyl-2H-tetrazole-5-acetic acid, ethyl ester acetaldehyde (step 1 of Example 9) (6.14 g, 22.4 mmol) in dichloromethane (100 mL) at −78° C. was added DIBAL (1.0 M in toluene, 50.0 mL, 50.0 mmol). The resulting mixture was stirred at −78° C. for 4 h. To the reaction mixture was added DIBAL (1.0 M in toluene, 25.0 mL, 25.0 mmol) and the resulting mixture was stirred at −78° C. for 8 h. To the mixture were added 2 M aqueous HCl (100 mL) and saturated aqueous NH4Cl (20 mL). The organic layer was separated, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (10:1) to give 3.45 g (67%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737163B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-559768ca584f4aa1b2ce50c1a9c6d2fc |
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| Source note | uspto-grants-2010_06 |
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