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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398003Generated: October 29, 2026

Sodium borohydride → HCID 11080708, compound

https://huagongshe.com/reaction/398003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23001298HCID 23001298—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 11080708HCID 11080708—

Reaction Steps

The product from Example 1, Step A (8.87 g, 20.2 mmol) was dissolved in methanol (50 mL) and methylene chloride (20 mL). Sodium borohydride (764 mg, 20.2 mmol) was added in portions at 0° C., and the solution was stirred for 2 hours. The reaction was quenched by the addition of saturated aqueous ammonium chloride until hydrogen evolution ceased. The resulting suspension was concentrated in vacuo and then partitioned between methylene chloride (50 mL) and saturated aqueous sodium bicarbonate (50 mL). The layers were separated and the aqueous layer was extracted with methylene chloride (3×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide the title product as a yellow oil which was sufficiently pure for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610722B2
Source datasetuspto-grants-2003_08
ORD IDord-d025209c2ceb469c87a959de64c4e453
Source noteuspto-grants-2003_08