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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991374Generated: October 30, 2026

Trimethyl orthoformate → HCID 59129101, compound

https://huagongshe.com/reaction/1991374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantPivalaldehydeHCID 12417—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 13338341HCID 13338341—
SolventAcetic AcidHCID 176—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 59129101HCID 59129101—

Reaction Steps

A mixture of 2,3,4,5-tetrahydro-1H-benzo[d]azepin-6-ol (see Demarinis et al. J. Med. Chem. 1984, 27, 918-921) (60 mg, 0.37 mmol), trimethylacetaldehyde (400 μL, 3.7 mmol), trimethyl orthoformate (390 μL, 3.7 mmol) and glacial acetic acid (40 μL) in 1-methyl-2-pyrolidinone (2.5 mL) was stirred at rt for 2.5 h. Sodium triacetoxyborohydride (388 mg, 1.8 mmol) was then added and the mixture was stirred at room temperature for 16 h. The mixture was then loaded on top of a silica gel-SCX (sulfonic acid) column and eluted first with methanol, then with 2 M ammonia in methanol. The latter fraction was evaporated and the resulting 3-neopentyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-6-ol was used in the next step without further purification. (M+H)+=234.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645778B2
Source datasetuspto-grants-2010_01
ORD IDord-4feabb8b311149d3ae7f36ffa03a02d9
Source noteuspto-grants-2010_01