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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740236Generated: October 31, 2026

Sodium Hydroxide → 3-(((Benzyloxy)carbonyl)amino)-3-methylbutanoic acid

https://huagongshe.com/reaction/1740236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-(((benzyloxy)carbonyl)amino)-3-methylbutanoateHCID 15042554—
SolventMethanolHCID 887—
Product3-(((Benzyloxy)carbonyl)amino)-3-methylbutanoic acidHCID 1455100799.7%

Reaction Steps

A solution of 18.3 g (68.9 mmol) of methyl 3-benzyloxycarbonylamino-3-methylbutanoate (Step B) in 20 mL of methanol at room temperature was treated dropwise with 51 mL of 2N NaOH (102 mmol, 1.5 eq). The mixture was stirred at room temperature for 16 hours then transferred to a separatory funnel and washed with hexane (3×). The aqueous layer was removed, cooled to 0° and slowly acidified to pH 2 (paper) by dropwise addition of 6N HCl. This mixture was extracted with ether (6×); combined extracts were washed with 1N HCl and brine, then dried over magnesium sulfate, filtered and solvent removed under vacuum to afford 17.3 g (68.7 mmol, 99%) of the product. 1H NMR (200 MHz, CDCl3): δ 1.42 (s, 6H), 2.77 (s, 2H), 5.06 (s, 2H), 5.2 (br s, 1H), 7.3 (s, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968924
Source datasetuspto-grants-1999_10
ORD IDord-d281576765754840bf521389d04e5b27
Source noteuspto-grants-1999_10